A-Cyst##R##(Rx)

What is A-CYST^® ?

A-CYST^® is a patented formulation designed for temporary replenishment of the glycosaminoglycan (GAG) layer in the urinary bladder. A-CYST^® contains naturally occurring components of the GAG layer of bladder epithelium. The GAG layer normally provides a protective barrier against microorganisms, carcinogens, crystals and other agents present in urine. The GAG layer has been identified as a primary defense mechanism from these irritants. Deficiencies in the GAG layer may affect epithelial barrier function and allow adherence of bacteria, microcrystals, proteins and ions, or movement of solute residues (i.e., urea).

The GAG layer of the bladder is deficient in cystitis. GAG deficiency contributes to clinical symptoms in diseases such as feline idiopathic cystitis (FIC), feline lower urinary tract disease (FLUTD), and cystitis caused by infections, trauma, urolithiasis, urinary retention and neoplasia.

A-CYST^® has been designed for use in cystitis to temporarily coat and help replenish the deficient GAG layer on bladder epithelium.

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

A-CYST^® is a patented formulation designed for temporary replenishment of the glycosaminoglycan (GAG) layer in the urinary bladder. A-CYST^® contains naturally occurring components of the GAG layer of bladder epithelium.

Benefits

• Reduced the overall 7-days repeat obstruction rate to 0%, versus a placebo group rate of 42% in a pilot study on intravesical infusion of A-CYST of blocked toms performed at the Colorado State University. ¹
• Helps replenish GAGs of the bladder epithelium with naturally occurring elements.
• Temporarily coats the bladder epithelium to help restore the barrier function.
• Versatile: can be administered to both cats and dogs

Resources

Bradley, A. M. and Lappin, M. R. (2014) ‘Intravesical glycosaminoglycans for obstructive feline idiopathic cystitis: a pilot study’, Journal of Feline Medicine and Surgery, 16(6), pp. 504–506

'Does intravesical infusion of glycosaminoglycans lessen the potential for repeat obstruction in male cats with suspected idiopathic cystitis?', Frequently Asked Questions Series, Colorado State University

Another Option for Managing Feline Cystitis

Withdrawal Period

No withdrawal period

Pack Size

AmproMed##T## For Calves

What is AmproMed^™ For Calves?

9.6% Oral Solution/Coccidiostat

Indications

An aid in the treatment and prevention of coccidiosis caused by Eimeria bovis and E. zuernii in calves.

Benefits

• Effective
  disrupts the coccidia life cycle
• Versatile
  approved for both the prevention and treatment of coccidiosis in beef and dairy calves
• Short withdrawal
  only 24 hours after the last administration
• Economical
  one gallon of concentrate treats 1,600 gallons of drinking water based on a 21-day prevention regimen
• Convenient
• treat the entire herd through the drinking water
• Easy to mix
  concentrated solution disperses readily into the drinking water
• Safe
  approved by FDA

Withdrawal Period

Withdraw 24 hours before slaughter. A withdrawal period has not been established for this product in pre-ruminating calves. Do not use in calves to be processed for veal.

Pack Size

AMPROMED##T## P FOR POULTRY

What is AmproMed^TM P for Poultry?

AmproMed^TM P for Poultry is an easy to use oral solution for treating coccidiosis in growing chickens, turkeys, and laying hens

Indications

AmproMed^TM P for Poultry 9.6% Oral Solution is intended for the treatment of coccidiosis in growing chickens, turkeys, and laying hens. If no improvement is noted within 3 days, have the diagnosis confirmed and follow the instructions of your veterinarian or poultry pathologist. Losses may result from intercurrent disease or other conditions affecting drug intake which can contribute to the virulence of coccidiosis under field conditions.

Benefits

• Effective
  Breaks up the coccidia life cycle
• Convenient
  Works in automatic drinking water proportioners to treat the entire flock
  Readily accepted by birds in the drinking water
• Economical
  At the recommended 0.012% level:
  • 1 gallon of oral solution treats 800 gallons of drinking water
  
• Safe
  approved by FDA

Withdrawal Period

None

Pack Sizes

BiloVet##R## Soluble Powder(Rx)

What is BiloVet^®?

A soluble powder for oral use in chickens, turkeys, swine and honey bees

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

Swines

For the treatment and control of swine dysentery (SD) associated with Brachyspira hyodysenteriae. For the treatment and control of swine dysentery associated with Brachyspira hyodysenteriae when followed immediately by tylosin phosphate Type A medicated article in feed. For the control of porcine proliferative enteropathies (PPE, ileitis) associated with Lawsonia intracellularis when followed immediately by tylosin phosphate Type A medicated article in feed.

Chickens

As an aid in the treatment of chronic respiratory disease (CRD) associated with Mycoplasma gallisepticum in broiler and replacement chickens. For the control of CRD associated with Mycoplasma gallisepticum at the time of vaccination or other stress in chickens. For the control of CRD associated with Mycoplasma synoviae in broiler chickens.

Turkeys

For the reduction in severity of the effects of infectious sinusitis associated with Mycoplasma gallisepticum.

Bees

For the control of American Foulbrood (Paenibacillus larvae).

Benefits

• Safe
  FDA Approved
• Versatile
  Available for use in multiple species – including chicken, turkey, swine, and honey bees
• Convenient
  Two package sizes to meet the varying demands of producers

Withdrawal Period

Additional Safety Information

• Administer the full dose and dosing regimen once medication is initiated.
• Use of BiloVet® or another macrolide is not advised if additional therapy is needed beyond the original course of medication.
• Avoid contact with human skin. When mixing and handling, use protective clothing and impervious gloves.

Pack Size

BiloVet##R##(RX)

What is BiloVet^® ?

BiloVet is an injectable antibiotic that contains 200 mg of tylosin per mL, a proven molecule that has been used as an effective treatment drug for a variety of conditions in both cattle and swine for over 30 years.

Indications

 

Beef Cattle and Non-Lactating Dairy Cattle

For the treatment of:

• bovine respiratory complex (shipping fever, pneumonia)
• foot rot (necrotic pododermatitis)
• calf diptheria
• metritis

 

Swine

For the treatment of:

• swine arthritis
• swine pneumonia
• swine erysipelas
• swine dysentery when followed by appropriate medication in the drinking water and/or feed

Benefits

• A versatile, cost-effective antibiotic for use in both cattle and swine
• Proven molecule, trusted for over 30 years
• Ready-to-use, no mixing or refrigeration required
• Same formulation as Tylan^® 200 injection

Withdrawal Period

Additional Safety Information

• If tylosin medicated drinking water is used as a follow-up treatment for swine dysentery, the animal should thereafter receive feed containing 40 to 100 grams of tylosin per ton for 2 weeks to assure depletion of tissue residues.
• Do not mix BiloVet with other injectable solutions as this may cause a precipitation of the active ingredients.
• Adverse reactions, including shock and death may result from overdosage in baby pigs.
• Do not attempt injection into pigs weighing less than 25 pounds (0.5 mL) with the common syringe. It is recommended that tylosin 50 mg/mL injection be used in pigs weighing less than 25 pounds.

Pack Size

Bimasone##T##

What is Bimasone?

Bimasone is an injectable form of flumethasone, a chemical modification of prednisolone which possesses greater anti-inflammatory and gluconeogenic properties than the parent compound when compared on an equivalent basis. Due to the potency of Bimasone, dosage recommendations should be consulted prior to drug administration.

Indications

Bimasone is recommended for the various rheumatic, allergic, dermatologic, and other disease states which are known to be responsive to the anti-inflammatory corticoids.

Flumethasone has the highest relative glucocorticoid activity (120) and long duration of effect compared to other commonly used corticosteroids.

RELATIVE POTENCIES OF COMMONLY USED CORTICOSTEROIDS

Benefits

• Bioequivalent to FluCort(R) (flumethasone)
• Consistent and Reliable - Non-compounded, Longer Shelf life
• Commercially Available
• Only FDA-approved Flumethasone ANADA # 200-612

Additional Safety Warnings

The close observation of animals under treatment with this drug is necessary.

Use of corticosteroids may result in inhibition of endogenous steroid production following drug withdrawal. 

Corticosteroids administered to animals may induce the first stage of parturition when administered during the last trimester of pregnancy. Corticosteroids administered to dogs, rabbits and rodents during pregnancy have resulted in cleft palate in offspring. Corticosteroids administered to dogs during pregnancy have also resulted in other congenital anomalies, including deformed forelegs, phocomelia and anasarca.

CONTRAINDICATIONS: Do not use in viral infections. Except for emergency therapy, do not use in animals with tuberculosis, chronic nephritis, cushingoid syndrome and peptic ulcers. Existence of congestive heart failure, diabetes and osteoporosis are relative contraindications.

Pack Size

Bimectin##R## Injection

What is Bimectin^® Injection?

Bimectin^® Injection is an excellent and effective choice for the treatment and control of a wide range of internal and external parasites of cattle and swine. Bimectin^® is absorbed quickly to reach and kill parasites, you can be confident when using Bimectin^® Injection as part of your parasite control strategy.

Bimectin^® Injection offers convenience, with only a single low-volume dose required to effectively treat and control a broad range of parasites which may impair the health of cattle and swine.  It is also cost effective; having an inexpensive cost-per-dose. Bimectin^® Injection is also FDA-approved.

Indications

Cattle

Effective treatment and control of harmful species of:

• gastrointestinal roundworms
• lungworms
• grubs
• sucking lice
• mange mites

Swine

Effective treatment and control of harmful species of:

• gastrointestinal roundworms
• lungworms
• lice
• mange mites

The table below details the specific parasites for which Bimectin^® is indicated.
Bimectin^® Injection is licensed for the treatment & control of the following harmful parasites:

Persistent Activity:

Ivermectin Injection has been proven to effectively control infections and to protect cattle from reinfection with Dictyocaulus viviparus and Oesophagostomum radiatum for 28 days after treatment; Ostertagia ostertagi, Trichostrongylus axei and Cooperia punctata for 21 days after treatment; Haemonchus placei and Cooperia oncophora for 14 days after treatment.

Benefits

• Broad Spectrum: effective against a wide range of external and internal parasites in beef cattle and swine
• Convenient: single, small volume dose required
• Effective: causes paralysis and death of parasites and helps prevent reinfection
• Package safety: rigid plastic vials provide for a firm grip and prevent breakage, individual vial cartons protect vial contents from sunlight
• Economical: inexpensive on a cost per dose basis
• Safe: approved by FDA

Withdrawal Period

Pack Sizes

BIMECTIN##R## PASTE

What is Bimectin^® Paste?

A proven anthelmentic and boticide Bimectin contains 1.87% ivermectin, providing the broadest spectrum activity against parasites and bots. Apple flavored and scented for excellent palatability and ease of dosing. The calibrated syringe allows accurate dosing and the gel formulation facilitates absorption.

The product is safe to use in horses of all ages including mares at any stage of pregnancy.

Indications

Bimectin^® (ivermectin) Paste 1.87% provides effective treatment and control of the following parasites in horses:

• Large Strongyles (adults)
  • Strongylus vulgaris (also early forms in blood vessels)
  • S. edentatus (also tissue stages)
  • S. equinus
  • Triodontophorus spp. including T. brevicauda, T. serratus
  • Craterostomum acuticaudatum
• Small Strongyles (adults, including those resistant to some benzimidazole class compounds)
  • Coronocylcus spp. including C. coronatus, C. labiatus and C. labratus
  • Cyathostomum spp. including C. catinatum, and C. pateratum
  • Cylicocyclus spp. incluidng C. insigne, C. leptostomum, C. nassatus and C. brevicapsulatus
  • Cylicodontophorus spp.
  • Cylicostephanus spp. including C. calicatus, C. goldi, C. longibursatus, C. minutus
  • Petrovinema poculatum
• Small Strongyles (fourth–stage larvae)
• Pinworms (adults and fourth–stage larvae)
  • Oxyuris equi
• Ascarids (adults and third– and fourth–stage larvae)
  • Parascaris equorum
• Hairworms (adults)
  • Trichostrongylus axei
• Large-mouth Stomach Worms (adults)
  • Habronema muscae
• Bots (oral and gastric stages)
  • Gasterophilus spp. including G. intestinalis and G. nasalis
• Lungworms (adults and fourth–stage larvae)
  • Dictyocaulus arnfieldi
• Intestinal Threadworms (adults)
  • Strongyloides westeri
• Summer Sores caused by Habronema and Draschia spp. cutaneous third-stage larvae
• Dermatitis caused by neck threadworm microfilariae, Onchocerca sp.

Benefits

• Apple flavored
• Approved for All Horses Over 6 Weeks: including mares at any stage of pregnancy
• Easy-to-use: Pre-measured plastic syringes provide accurate dosing
• Proven: Contains ivermectin, a proven anthelmintic and Boticide

How to Use

Withdrawal Period

Do not use in horses intended for human consumption

Pack Size

BIMECTIN##R## PLUS INJECTION

What is Bimectin^® Plus Injection?

Bimectin^® Plus Injection (ivermectin and clorsulon) is an injectable parasiticide for cattle. One low-volume dose effectively treats and controls the following internal and external parasites that may impair the health of cattle: gastrointestinal roundworms (including inhibited Ostertagia ostertagi), lungworms, adult liver flukes, grubs, sucking lice, and mange mites. The dosage level of clorsulon supplied by Bimectin^® Plus Injection is effective only against adult liver flukes (Fasciola hepatica).

Indications

Bimectin^® Plus is indicated for the effective treatment and control of the following parasites in cattle:

Benefits

• Broad spectrum treatment and control of internal and external parasites in cattle
• Convenient single, small dose required
• Effective: causes paralysis and death of parasites and helps prevent reinfection
• Package safety: rigid plastic vials provide for a firm grip and prevent breakage, individual vial cartons protect vial contents from sunlight
• Cost effective parasitic control in your herd
• FDA approved

Withdrawal Period

Pack Size

Bimectin##R## Pour-on

What is Bimectin^® Pour-On?

Bimectin^® (ivermectin) Pour-On contains 5 mg of ivermectin per mL and delivers effective, long-lasting control against a wide range of internal and external parasites in cattle, in one convenient low-volume application. Bimectin^® Pour-On penetrates quickly to reach and kill parasites, and also offers long-activity against them. The Pour-On presentation facilitates ease of application and reduced stress on treated animals, and is also Beef Quality Assurance-friendly, since no injection is required.

Bimectin^® Pour-On is well tolerated by breeding animals and is also available in five different package sizes, to meet a variety of producer needs. It is also FDA approved.

Indications

Bimectin^® Pour-On is indicated for the effective treatment and control of Gastrointestinal Roundworms, Lungworms, Cattle Grubs, Mites, Lice and Horn Flies.

Bimectin^® Pour-on is indicated for the treatment and control of the following specific parasites:

Benefits

• Broad spectrum control against a wide range of internal and external parasites
• Rapid penetration to reach and kill target parasites quickly
• Provides persistent, lasting activity against economically relevant parasites
• Convenient, pour-on formulation that causes less stress on the animal

How to Use

Withdrawal Period

Pack Sizes

BOVitalize##T##

Indications

A supplement of trace minerals and vitamins to aid in providing nutrients needed to support a healthy immunity and maintain health.

Features + Benefits

ROLES CRITICAL OF MICRONUTRIENTS AT KEY LIFE STAGES

PROS AND CONS OF DIFFERENT ROUTES OF ADMINISTRATION

Supplements can be provided through several different routes of administration, each has its own advantages and disadvantages:

THE ROLE OF KEY NUTRIENTS IN CATTLE

TARGET

REPRODUCTION + FERTILITY
IMMUNE FUNCTION
GROWTH + DEVELOPMENT

DEFICIENCY

REDUCED GROWTH
POOR REPRODUCTIVE PERFORMANCE
CARDIAC FAILURE

TARGET

REPRODUCTION + FERTILITY
DISEASE RESISTANCE
HAIR COLOR

DEFICIENCY

REDUCED FERTILITY
CARDIAC FAILURE
WEAK BONES

TARGET

REPRODUCTION + FERTILITY
HEALTHY FEET + HOOVES
HEALTHY SKIN + COAT

DEFICIENCY

HAIR LOSS
SKIN ABNORMALITIES
HOOF ABNORMALITIES

TARGET

REPRODUCTIVE PERFORMANCE
IMMUNE FUNCTION
VISION

DEFICIENCY

POOR REPRODUCTIVE PERFORMANCE
INCREASED INFECTIONS

TARGET

REPRODUCTIVE PERFORMANCE
IMMUNE FUNCTION
GROWTH

DEFICIENCY

REDUCED GROWTH
POOR REPRODUCTIVE PERFORMANCE
CARDIAC FAILURE + INFECTIONS

COMPARATIVE PHARMACOKINETICS BETWEEN ORAL AND INJECTABLE SUPPLEMENTATION

Animals: 20 head – 660 pound beef cattle replacement heifers
Treatment A (n=10): *BOV Oral (5 mL/220 pounds)
Treatment B (n=10): Multimin^® 90 Injection (1 mL/100 pounds)
Plasma Collected at 0, 24, 48 and 72-hour intervals

Results and Conclusion:
On arrival: Calves were deficient in Selenium and Vitamin E, marginal in Copper and Vit A
Calves treated with *BOV Oral responded by increased Copper, Selenium, Vitamin A and E
No difference was demonstrated between Zinc levels through 72 hours with BOVitalize and MultiMin

COMPARISON OF BOVITALIZE TO OTHER SUPPLEMENTS IN DIFFERENT CLASSES OF CATTLE

WEANED 500 POUND CALF

1,000 POUND YEARLING

2+ YEAR OLD COW

*Profusion is a registered trademark of ZINPRO Eden Prairie, MN.

Pack Size

BUTATRON##R## TABLETS (Rx)

What are Butatron^® Tablets?

Butatron^® Tablets are anti-inflammatory tablets that provide effective pain relief to both horses and dogs.

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

Butatron^® tablets are indicated for the management of musculoskeletal conditions such as osteoarthritis, particularly where continued mobility is considered desirable.

Phenylbutazone possesses non-hormonal, anti-inflammatory activity of value in the management of musculoskeletal conditions in dogs and horses such as the arthritides, including osteoarthritis, and as an aid in the relief of inflammation associated with intervertebral disc syndrome in dogs.

Benefits

• Rapid onset of activity: usually provides relief within 24 hours
• Proven: safe and effective
• Versatile: treats inflammatory conditions in both dogs and horses
• Safe: approved by FDA

Additional Safety Information

• Phenylbutazone should not be administered to animals with serious hepatic, renal or cardiac pathology, or those with a history of blood dyscrasia.
• Phenylbutazone should not be administered to meat, egg or milk producing animals because the status of residues of drug remaining in edible tissues has not been determined.
• Use with caution in animals with a history of drug allergy.
• Stop medication at the first sign of gastrointestinal upset, jaundice or blood dyscrasia.

Pack Size

ClindaMed##T## (Rx)

What is ClindaMed^™?

ClindaMed^™ Oral Drops is a palatable formulation intended for oral administration. Each mL of ClindaMed^™ Oral Drops liquid contains clindamycin hydrochloride equivalent to 25 mg clindamycin; and ethyl alcohol, 8.64%.

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

ClindaMed^™ Oral Drops (for use in dogs and cats) are indicated for the treatment of infections caused by susceptible strains of the designated microorganisms in the specific conditions listed below:

Dogs

• Skin infections (wounds and abscesses)
  due to coagulase positive staphylococci (Staphylococcus aureus or Staphylococcus intermedius).
• Deep wounds and abscesses
  due to Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium necrophorum and Clostridium perfringens.
• Osteomyelitis
  due to Staphylococcus aureus, Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium necrophorum and Clostridium perfringens

Cats

• Skin infections (wounds and abscesses)
  due to Staphylococcus aureus, Staphylococcus intermedius, Streptococcus spp
• Deep wounds and abscesses
  due to Clostridium perfringens and Bacteroides fragilis
• Dental infections
  due to Staphylococcus aureus, Staphylococcus intermedius, Streptococcus spp., Clostridium perfringens and Bacteroides fragilis

Benefits

• Highly effective
• Multiple indications for both dogs and cats
• Palatable
• Generally well tolerated by the animal
• Ready to use
• Single daily dose in cats
• No refrigeration required
• Dropper included for accurate, safe administration

Additional Safety Information

• Contraindicated in animals with a history of hypersensitivity to preparations containing clindamycin or lincomycin.
• Because of potential adverse gastrointestinal effects, do not administer to rabbits, hamsters, guinea pigs, horses, chinchillas or ruminating animals.
• Patients with severe renal disease and/or severe hepatic disease accompanied by severe metabolic aberrations should be dosed with caution.
• Clindamycin hydrochloride has been shown to have neuromuscular blocking properties that may enhance the action of other neuromuscular blocking agents. Use with caution in animals receiving such agents.
• During prolonged therapy of one month or greater, periodic liver and kidney function tests and blood counts should be performed.
• Safety in gestating bitches and queens or breeding male dogs and cats has not been established.

Pack Size

Confidence EQ##R##

What is Confidence EQ^®?

Confidence EQ^® is an equine appeasing pheromone 1% gel that has been clinically proven to reduce stress in horses facing new and challenging environments. Pheromones are chemical signals exchanged between members of the same animal species. They are a form of communication that trigger various behaviors, such as alarm, reproduction, territory marking and mother-baby bonding. They are not odors or hormones, so they do not affect cell function.

Mares release an equine appeasing pheromone (EAP) towards their nursing foal. Confidence EQ^® replicates this pheromone, offering the same behavioral benefits in horses of all ages:

• Provides reassurance and emotional stabilization.
• Signifies a safe and secure environment.
• Signifies a safe and secure environment.

Mimics Mare Signal to Her Foal

By replicating the soothing pheromone signal a mare sends to her nursing foal, Confidence EQ^® speaks to your horse in a language they instinctually understand.

See it at Work

Some horses may raise their upper lip after application, a reaction called the Flehman response; this natural behavior is how horses receive and interpret the pheromones, and could be the first indication that Confidence EQ^® is working.

Clinically Proven to Calm

In a clinical study, horses treated with an application of Confidence EQ^® had less stress as measured by heart rate, salivary cortisol, frequency of vocalization, fecal water loss and behavior.¹

Indications

Confidence EQ® replicates the equine appeasing pheromone that mares produce as they nurse their foal. In adult horses, the presence of this pheromone is a signal that the environment is safe and secure, which can facilitate learning.

How Does Confidence EQ^® Work?

Point Point Point

Benefits

Confidence EQ^® pheromone 1% gel can help reduce the behavioral and physiological symptoms of stress in horses of any age.

• Training tool – Can be combined with behavioral and desensitization therapy.
• Safe for competition – Not listed on the FEI prohibited substance list.
• Fast & long-lasting – Takes effect in 30 minutes, lasts 2.5 hours, and can be reapplied as needed.
• Single-use packets – Ensure accurate dose every time.
• Easy to administer – No syringes, mixing food, pills or other uncomfortable application methods that can add stress to the horse.

When To Use Confidence EQ^®

Horses are sensitive to their environment and can overreact when faced with stressful situations such as:

Transportation

Training

Medicating /
Veterinarian Visits

New Environment or
Change in Routine

Farrier Visits

Maiden Mares /
Weaning

Social Separation

Competing

Horses in these situations may show signs of stress such as pawing, vocalizing, flared nostrils, kicking, lack of concentration, and resistance. These behavioral changes are due to an elevated cortisol level, which when prolonged, also triggers multiple physiological responses like increased heart rate and blood pressure, weakening of the immune system, cribbing, and digestive issues—all of which can develop into significant problems for owners, trainers and veterinary practitioners.

Instilling confidence with Confidence EQ^® pheromone is a proven way to help horses deal with new or unexpected stimuli.

How To Apply

ConfidenceEQ is easy and quick to apply. There are no syringes, mixing food, pills or other uncomfortable application methods that can be difficult to administer or add stress to your horse. Takes effect in 30 minutes, lasts 2.5 hours, and can be reapplied as needed.

Apply 30 minutes before stressful situation.

Put gel on fingers.

Open the gel packet.

Apply at the base of the nostrils.

Confidence EQ - Pamela Spatz

I have a colt who was feral when I rescued him but progressed wonderfully through his training. When it came time to move him to a new pasture, I was very apprehensive about trailering. He only had one trailering experience in his life, and it was coming to me from where he was captured — it didn’t go well. I heard great things about Confidence EQ® from my veterinary customers who use it in their practices, and I had a sample packet on hand. So, I decided to use it before we trailered him. I am still in shock as to how smoothly things went. My little formerly feral colt walked up and looked at the trailer, alert yet relaxed. He stood there for a moment, and then followed me into the trailer like a seasoned pro! I love that he was tranquil but not tranquilized. He was well aware of what was going on, but comfortable and taking it all in. It was truly a learning experience for him! As a Henry Schein Animal Health representative, I can now wholeheartedly endorse Confidence EQ with a personal experience to back it up!

PAMELA SPATZ, ANIMAL HEALTH DISTRIBUTOR REPRESENTATIVE

Transportation

New Environments

Confidence EQ - Brenda Madsen

While on a ride, my horse and I were attacked by an unbroken six-year-old Arabian stud who had gotten away from his owner. We were both traumatized. He wouldn't even go past our property when I tried to ride him a couple of days after the incident. I called my veterinarian to see if there was anything I could give him to help him get through this trauma. He recommended ConfidenceEQ. The first time I used it on him, it was evident he was easier to work with. We can now go on our favorite trails without him shaking, flaring his nostrils, repeatedly backing up and basically refusing to go off of our property. I would highly recommend ConfidenceEQ to anyone having problems with their horses due to fearful or traumatic situations; it really works!

BRENDA MADSEN, TRAIL RIDER

Training

Vet Visits

Confidence EQ - Nathan Slovis

I have used Confidence EQ many times and am very pleased with this product. I have used it with my own anxious horses that consistently paw and damage the floor mats in the trailer when going to a show. I found that when using Confidence EQ they looked relaxed when unloading. In addition, I also have used it on animals that would not enter a starting gate and horses that I am moving away from companions to a new barn. Typically these horses would pace the stall when separated from friends. With Confidence EQ they eat well and are comfortable. These are just a few instances where I have used this product successfully. I recommend this product as a useful tool in helping horses manage stressful situations.

NATHAN SLOVIS, DVM, DIPL. ACVIM, CHT (CERTIFIED HYPERBARIC TECHNOLOGIST)
HAGYARD EQUINE MEDICAL INSTITUTE

Transportation

New Environments

Vet Visits

Social Separation

Confidence EQ - Christy Burleson

In the last few years, my horse has developed a gate issue. Once, my horse reared straight up and jumped — very dangerous! After that episode, my veterinarian of 20 years recommended trying ConfidenceEQ. Now, my horse is well behaved at the gate, which gives us the best chance for a good, clean run. All my competitors have noticed the change and are talking about how good he’s going in. This is the most incredible product I have ever used! My horse is now respectful at the gate, and it makes competing much more enjoyable.

CHRISTY BURLESON, BARREL RACER

Training

Vet Visits

Competing

Confidence EQ - Georgana Wilpizeski

I rarely trailer my horse. When I do, the experience is uncomfortable at best. At worst, he will rear, buck and kick when attempting to load. I used a sample of ConfidenceEQ, followed the directions and watched in amazement as my gelding walked right on the trailer. He was alert, aware and had a happy — almost eager — expression on his face. He was quiet the whole trip and unloaded perfectly. I recommend this product without reservation.

GEORGANA WILPIZESKI, TRAIL RIDER

Transportation

New Environments

Social Separation

Confidence EQ - Andrea McKim

I was skeptical that ConfidenceEQ would work on my 10-year-old, off-the-track Thoroughbred gelding. He was inconsolable when separated from his stablemate — running and screaming for her until utterly exhausted. Letting them be together at pasture only reinforced the bond. ConfidenceEQ helped with his anxiety. After two weeks of use prior to afternoon pasture time, he is a completely normal horse. I’m amazed! No more drama around here! Around our ranch, we refer to it as ‘mama gel.’

ANDREA MCKIM, DRESSAGE RIDER

New Environments

Social Separation

Confidence EQ - Bonnie Bingham

I used a sample of ConfidenceEQ yesterday on my Friesian/Arabian cross, and we had the most comfortable ride ever. ConfidenceEQ allowed him to focus on our training and diminished distractions. I’m totally amazed and ordered more this morning. What a great training tool. Thank you, thank you!

BONNIE BINGHAM, TRAIL RIDER

Training

Confidence EQ - Dani Sussman

I have been using Confidence EQ for the last month and couldn't be happier with the results. My horse Kaptain America is very sensitive and can get distracted very easily. I find Confidence EQ allows him to be more focused on the task at hand, and therefore giving a better performance.

DANI SUSSMAN, INTERNATIONAL LEVEL 3-DAY EVENT RIDER

Training

Competing

Confidence EQ - DL Bovi

My 23-year-old thoroughbred lost an eye three years ago and he has had a difficult adjustment. I have used ConfidenceEQ to help him feel more relaxed under the saddle and when we go to the veterinarian's clinic. He responds nicely.

DL BOVI, RIDER

Farrier Visits

Pack Size

Custom Vaccines

Detomequin##T## (RX)

What is Detomequin^®?

Detomequin^® is indicated for use as a sedative and analgesic to facilitate minor surgical and diagnostic procedures in mature horses and yearlings.

Indications

Detomequin^® is indicated for use as a sedative and analgesic to facilitate minor surgical and diagnostic procedures in mature horses and yearlings. It has been used successfully for the following: to calm fractious horses, to provide relief from abdominal pain, to facilitate bronchoscopy, bronchoalveolar lavage, nasogastric intubation, nonreproductive rectal palpations, suturing of skin lacerations, and castrations. Additionally, an approved, local infiltration anesthetic is indicated for castration.

Benefits

• Bioequivalent to Dormosedan® Sterile Solution (detomidine hydrochloride).
• Cost-effective alternative.
• Allows dosing flexibility so you can accurately regulate the depth and length of sedation and analgesia.

Withdrawal Period

NA

Dexium##R## (Rx)

What is Dexium^®?

Dexamethasone Solution is a synthetic analogue of prednisolone, having similar but more potent anti-inflammatory therapeutic action and diversified hormonal and metabolic effects.

Each mL contains 2 mg dexamethasone, 500 mg polyethylene glycol 400, 9 mg benzyl alcohol, 1.8 mg methylparaben and 0.2 mg propylparaben as preservatives, 4.75% alcohol, HCI to adjust pH to approximately 4.9, water for injection q.s.

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

Dexium^® is indicated for the treatment of primary bovine ketosis and as an anti-inflammatory agent in the bovine and equine. 

As supportive therapy, Dexium^® may be used in the management of various rheumatic, allergic, dermatologic, and other diseases known to be responsive to anti- inflammatory corticosteroids. Dexium^® may be used intravenously as supportive therapy when an immediate hormonal response is required.

Benefits

• Potent: Approximately 20 times the anti-inflammatory activity of prednisolone and 70 to 80 times that of hydrocortisone
• Multi-species usage: Effective treatment for cattle and horses
• Fast absorption and powerful effect
• Choice of administration: IV or IM
• Safe: Approved by FDA

Withdrawal Period

A withdrawal period has not been established for this product in pre-ruminating calves. Do not use in calves to be processed for veal.

Additional Safety Information

• Clinical and experimental data have demonstrated that corticosteroids administered orally or parenterally to animals may induce the first stage of parturition when administered during the last trimester of pregnancy and may precipitate premature parturition.
• Except for emergency therapy, do not use in animals with chronic nephritis and hyper-corticalism (Cushing’s syndrome). Existence of congestive heart failure, diabetes, and osteoporosis are relative contraindications. Do not use in viral infections during the viremic stage.
• Overdosage of some glucocorticoids may result in sodium retention, fluid retention, potassium loss, and weight gain.
• Doses greater than those recommended in horses may produce transient drowsiness or lethargy in some horses.
• Use of corticosteroids, depending on the dose, duration, and specified steroid, may result in inhibition of endogenous steroid production following drug withdrawal.

Pack Size

Dexium-SP##T## (Rx)

What is Dexium-SP^™?

Dexamethasone sodium phosphate (a synthetic adrenocortical steroid), is a white or slightly yellow crystalline powder. It is freely soluble in water and is exceedingly hygroscopic.

Each mL of sterile aqueous solution contains Dexamethasone Sodium Phosphate 4 mg (equivalent to dexamethasone 3 mg), Sodium Citrate 10 mg, Sodium Bisulfite 2 mg, Benzyl Alcohol 1.5% as preservative, in Water for Injection q.s., Sodium Hydroxide and/or Hydrochloric Acid to adjust pH to between 7.0 and 8.5.

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

Dexamethasone sodium phosphate injection is indicated as a rapid adrenal glucocorticoid and/or anti-inflammatory agent in horses.

Benefits

• Concentrated: Relatively large amount of active ingredient in small volume of solution
• Fast acting: Rapid onset of activity
• Economical: Effective at low dosages
• Safe: Approved by FDA

Withdrawal Period

Do not use in horses intented for food.

Additional Safety Information

• Clinical and experimental data have demonstrated that corticosteroids administered orally or by injection to animals may induce the first stage of parturition if used during the last trimester of pregnancy and may precipitate premature parturition.
• Do not use in viral infections.
• Except when used for emergency therapy, dexamethasone sodium phosphate is contraindicated in animals with tuberculosis and chronic nephritis. Existence of congestive heart failure, osteoporosis and diabetes are relative contraindications.
• Overdosage of some glucocorticoids may result in sodium retention, fluid retention, potassium loss and weight gain.

Pack Size

EnroMed##R## 100

Cattle Swine

A STERILE, READY-TO-USE INJECTABLE FLUOROQUINOLONE TO TREAT AND CONTROL BOVINE RESPIRATORY DISEASE (BRD)

Mannheimia haemolytica

Pasteurella multocida

Histophilus somni

Mycoplasma bovis

• FDA-approved bioequivalent to Baytril 100^®
• Cost-effective BRD treatment + control
• Approved for single-dose and multi-day treatment and control

A STERILE, READY-TO-USE INJECTABLE FLUOROQUINOLONE TO TREAT AND CONTROL SWINE RESPIRATORY DISEASE (SRD)

Actinobacillus pleuropneumoniae

Pasteurella multocida

Haemophilus parasuis

Streptococcus suis

Bordetella bronchiseptica

Mycoplasma hyopneumoniae

• FDA-approved bioequivalent to Baytril 100^®
• Cost-effective SRD treatment + control
• Approved for colibacillosis control in weaned pigs

Equimax##R##

What is Equimax^®?

Equimax^® is a broad spectrum parasite, bot and tapeworm control. It is safe to use in foals as early as 4 weeks of age, pregnant and lactating mares, and breeding stallions.

Indications

Equimax^® has broad-spectrum activity against a range of debilitating and performance-depriving parasites including:

• Tapeworms (Anoplocephala perfoliata)
• Large Strongyles (adults) (Strongylus vulgaris) also early forms in blood vessels), (S. edentatus) (also tissue stages), (S. equinus), (Triodontophorus spp.)
• Small Strongyles (adults, including those resistant to some benzimidazole class compounds) (Cyathostomum spp.), (Cylicocyclus spp.), (Cylicostephanus spp.), (Cylicodontophorus spp.)
• Small Strongyles (fourth–stage larvae)
• Pinworms (adults and fourth–stage larvae) (Oxyuris equi)
• Ascarids (adults and third– and fourth–stage larvae) (Parascaris equorum)
• Hairworms (adults) (Trichostrongylus axei)
• Large-mouth Stomach Worms (adults) (Habronema muscae)
• Bots (oral and gastric stages) (Gasterophilus spp.)
• Lungworms (adults and fourth–stage larvae) (Dictyocaulus arnfieldi)
• Intestinal Threadworms (adults) (Strongyloides westeri)
• Summer Sores caused by Habronema and Draschia spp. cutaneous third-stage larvae
• Dermatitis caused by Neck Threadworm microfilariae, Onchocerca sp.

Benefits

How to Use

Withdrawal Period

Do not use in horses intended for human consumption.

Pack Size

Exodus##R##

What is Exodus^®?

Exodus^® Paste (pyrantel pamoate) is a pale yellow to buff paste containing 43.9% w/w pyrantel pamoate in an inert vehicle. Each syringe contains 3.6 grams pyrantel base in 23.6 grams paste. Each milliliter contains 171 milligrams pyrantel base as pyrantel pamoate.

Indications

For the removal and control of mature infections in horses and ponies of large strongyles (Strongylus vulgaris, S. edentatus, S. equinus); small strongyles; pinworms (Oxyuris equi); and large roundworms (Parascaris equorum) in horses and ponies.

Benefits

• Apple flavored
• Proven: Contains pyrantel pamoate for safe worm removal and control
• Versatile: Over 90% effective against most major equine worms
• Convenient: Pre-measured plastic syringes provide accurate dosing
• Easy-to-Use: Available in two size syringes

Withdrawal Period

Not intended for use in horses intended for human consumption.

Pack Size

Flunazine##R## (Rx)

What is Flunazine^®?

Flunixin Meglumine is a potent, non-narcotic, nonsteroidal analgesic agent with anti-inflammatory and antipyretic activity. Each milliliter of Flunazine^® Injectable Solution contains flunixin meglumine equivalent to 50 mg flunixin, 0.1 mg edetate disodium, 2.2 mg sodium formaldehyde sulfoxylate, 4.0 mg diethanolamine, 207.2 mg propylene glycol, 5.0 mg phenol as preservative, hydrochloric acid, water for injection q.s.

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

Horse

• Recommended for the alleviation of inflammation and pain associated with musculoskeletal disorders in the horse
• Recommended for the alleviation of visceral pain associated with colic in the horse

Cattle

• Indicated for the control of pyrexia associated with bovine respiratory disease, endotoxemia and acute bovine mastitis.
• Indicated for the control of inflammation in endotoxemia.

Benefits

• Significantly more pain relief than pentazocine, meperidine and codeine
• Offers quick onset of effective analgesic activity, within 2 hours of administration
• Active up to 36 hours
• Non-narcotic, non-steroidal, no adverse reactions when used as directed
• Indicated for horses and cattle
• Approved by FDA

Withdrawal Period

Additional Safety Information

• In horses, isolated reports of local reactions following intramuscular injection, particularly in the neck, have been received. In rare instances in horses, fatal or nonfatal clostridial infections or other infections have been reported in association with intramuscular use of flunixin meglumine.
• In horses and cattle, rare instances of anaphylactic-like reactions, some of which have been fatal, have been reported, primarily following intravenous use.
• In horses, intra-arterial injection should be avoided.
• In cattle, do not use in animals showing hypersensitivity to flunixin meglumine. Use judiciously when renal impairment or gastric ulceration are suspected.
• In horses, the effect of Flunazine® Injectable Solution on pregnancy has not been determined.
• In cattle, do not use in bulls intended for breeding, as reproductive effects of Flunazine® Injectable Solution in these classes of cattle have not been investigated.
• Do not use in horses intended for human consumption.
• Since many NSAIDs possess the potential to induce gastrointestinal ulceration, concomitant use of Flunazine® Injectable Solution with other anti-inflammatory drugs, such as other NSAIDs and corticosteroids, should be avoided or closely monitored.

Pack Size

FLUNAZINE##R## EQUINE PASTE (Rx)

What is Flunazine^® Equine Paste?

Flunixin Meglumine is a potent, non-narcotic, nonsteroidal analgesic agent with anti-inflammatory and antipyretic activity. A syringe containing flunixin meglumine equivalent to 1500 mg flunixin

Indications

Apple-flavored oral paste for the alleviation of inflammation and pain associated with musculoskeletal disorders in the horse.

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Benefits

• Significantly more pain relief than pentazocine, meperidine and codeine
• Offers quick onset of effective analgesic activity, within 2 hours of administration
• Active up to 36 hours
• Non-narcotic, non-steroidal, no adverse reactions when used as directed
• Apple flavored for ease of oral administration
• Approved by FDA

Withdrawal Period

Do not use in horses intended for human consumption.

Additional Safety Information

• The effect of flunixin meglumine on pregnancy has not been determined.
• Do not use in horses intended for human consumption
• Flunixin meglumine treatment should not exceed 5 consecutive days.

Pack Size

Flunazine##R##-S (Rx)

What is Flunazine^®-S?

Flunixin Meglumine is a potent, non-narcotic, nonsteroidal analgesic agent with anti-inflammatory and antipyretic activity. Each mL of Flunazine^®-S (flunixin meglumine) Injectable Solution contains flunixin meglumine equivalent to 50 mg flunixin, 0.1 mg edetate disodium, 2.2 mg sodium formaldehyde sulfoxylate, 4.0 mg diethanolamine, 207.2 mg propylene glycol, 5.0 mg phenol as preservative, hydrochloric acid, water for injection q.s.

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

Flunazine^®-S (flunixin meglumine) Injectable Solution is indicated for the control of pyrexia associated with swine respiratory disease.

Benefits

• Reduces fever: pigs feel better which results in better performance.
• Fast acting: in as little as 0.4 hours post administration
• Long lasting: quantifiable drug concentration can be measured up to 18 hours
• Potent: more relief than with pentazocine, meperidine or codeine
• Safe: Non-narcotic, non-steroidal; no known contraindica- tions when used as directed

Withdrawal Period

Additional Safety Information

• Do not use in animals showing hypersensitivity to flunixin meglumine.
• Use judiciously when renal impairment or gastric ulceration is suspected.
• As a class, cyclo-oxygenase inhibitory NSAIDs may be associated with gastrointestinal, renal and hepatic toxicity. Concurrent administration of potentially nephrotoxic drugs should be carefully approached.
• NSAIDs may inhibit the prostaglandins that maintain normal homeostatic function.
• Concomitant use of flunixin meglumine with other anti-inflammatory drugs, such as other NSAIDs and corticosteroids, should be avoided.
• Not for use in breeding swine.
• Intramuscular injection may cause local tissue irritation and damage.

Pack Size

GENTAMED##T## SOLUBLE POWDER (Rx)

What is GentaMed™?

GentaMed™ is an antibacterial soluble power, to be administered in swine drinking water for indicated diseases.

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

GentaMed™ Soluble Powder is recommended for the control and treatment of colibacillosis in weanling swine caused by strains of E. coli sensitive to gentamicin, and for the control and treatment of swine dysentery associated with Brachyspira hyodysenteriae.

EACH g CONTAINS: Gentamicin sulfate equivalent to 333.33 mg gentamicin base.

Benefits

• Effective
  Stays in the GI tract to fight infection
• Versatile
  Approved to control and treat swine Colibacillosis and Dysentery
• Economical
  One scoop medicates 240 gallons of drinking water to treat and control colibacillosis at a concentration of the 25 mg/gal
• Convenient
  Treats large numbers of swine through drinking water
• Easy To Use
  Packaged in screw-top, moisture resistant jars for easy opening and closing
• Safe
  approved by FDA

Withdrawal Periods

Additional Safety Information

• Concentration of medication should be adjusted in extremely hot or cold weather to ensure correct dosage
• For swine dysentery, if the condition recurs, the medication may be repeated.  Ensure a control program is used following treatment.
• Medicated drinking water should not be stored or offered in rusty containers.
• There are no known contraindications to this drug when used as directed.

Pack Size

KetoMed##T##(RX)

What is KetoMed^™?

KetoMed (ketoprofen) is recommended for the alleviation of inflammation and pain associated with musculoskeletal disorders in horses. It is an FDA-approved non-narcotic, non-steroidal anti-inflammatory agent with analgesic and antipyetic properties.

Indications

KetoMed is recommended for the alleviation of inflammation and pain associated with musculoskeletal disorders in horses.

Benefits

PROTECT YOUR INVESTMENT WITH OUR SHATTERPROOF PLASTIC BOTTLE

BIOEQUIVALENT TO KETOFEN® STERILE SOLUTION

APPROVED BY FDA UNDER ANADA # 200-625

• Significantly reduces hoof pain associated with chronic laminitis for up to six hours¹
• Showed significant intra-articular anti-inflammatory activity in an experimentally induced acute carpal synovitis model²
• Therapeutically equivalent to flunixin meglumine in the alleviation of pain in carpal model of arthritis³
• NSAID of the propionic acid class that includes ibuprofen, naproxen and fenoprofen

1 - Owens JG, Kamerling SG, Stanton SR, Keowen ML. Effects of ketoprofen and phenylbutazone on chronic hoof pain and lameness in the horse. Equine Vet J. 1995;27(4):296-300.
2 - Owens JG, Kamerling SG, Barker SA. Pharmacokinetics of ketoprofen in healthy horses and those with acute synovitis. J Vet Pharmacol Ther. 1995;18(3):187-195.
3 - Longo E, Autefage A, Bayle R, Keister M, Van Gool E. Efficacy of a nonsteroidal anti- inflammatory, ketofen 10% (ketoprofen) in the treatment of colic in horses. J Equine Vet Sci. 1992;12(5):311-315.

Additional Safety Warnings

• Do not use in horses intended for human consumption
• This product should not be used in breeding animals since the effects of KetoMed on fertility, pregnancy or fetal health in horses have not been determined.
• Intra-arterial injection should be avoided.
• Do not use in horses previously showing hypersensitivity to ketoprofen.

Pack Size

LevaMed##T##

LevaMed##T## Soluble Pig Wormer

What is LevaMed^™ Soluble Pig Wormer?

LevaMed^™ Soluble Pig Wormer is a broad spectrum athelmintic for use in swine drinking water.

Indications

LevaMed^™ (levamisole hydrochloride) Soluble Pig Wormer is a broad-spectrum anthelmintic and is effective against the following nematode infections in swine.

• Large Roundworms: (Ascaris suum)
• Nodular Worms: (Oesophagostomum spp.)
• Lungworms: (Metastrongylus spp.)
• Intestinal Threadworms: (Strongyloides ransomi)

Benefits

• Broad spectrum: Effective against a variety of nematodes
• Economical: One 20.17 g bottle treats 200 - 25 lb pigs
• Short withdrawal: Only 72 hours after the last administration
• Oral dosage form: Reduces handling and animal stress
• Convenient packaging: Easy-on, easy-off screw-top plastic bottle serves as both mixing and storage bottle
• Safe: Approved by FDA

Withdrawal Period

Pack Size

LINCOMED##R## 100 (RX)

What is LincoMed^® 100?

LincoMed^® contains lincomycin hydrochloride, an antibiotic produced by Streptomyces lincolnensis var. lincolnensis, which is chemically distinct from all other clinically available antibiotics.

CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

LincoMed^® is indicated for the treatment of infectious forms of arthritis caused by organisms sensitive to its activity. This includes most of the organisms responsible for the various infectious arthritides in swine, such as staphylococci, streptococci, Erysipelothrix and Mycoplasma spp.

It is also indicated for the treatment of mycoplasma pneumonia.

Benefits

• Effective: Contains the proven antibiotic lincomycin in injectable form
• Safe: Approved by FDA

Withdrawal Period

Additional Safety Information

• The use of LincoMed 100 is contraindicated in animals previously found to be hypersensitive to the drug.
• Intramuscular injection may cause a transient diarrhea or loose stools.
• Not for use in swine weighing 300 pounds or more.

Pack Size

LINCOMED##R## 300 (RX)

What is LincoMed^® 300?

LincoMed^® contains lincomycin hydrochloride, an antibiotic produced by Streptomyces lincolnensis var. lincolnensis, which is chemically distinct from all other clinically available antibiotics.

CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

LincoMed^® is indicated for the treatment of infectious forms of arthritis caused by organisms sensitive to its activity. This includes most of the organisms responsible for the various infectious arthritides in swine, such as staphylococci, streptococci, Erysipelothrix and Mycoplasma spp.

It is also indicated for the treatment of mycoplasma pneumonia.

Benefits

• Effective: Contains the proven antibiotic lincomycin in injectable form
• Safe: Approved by FDA

Withdrawal Period

Additional Safety Information

• The use of LincoMed 300 is contraindicated in animals previously found to be hypersensitive to the drug.
• Intramuscular injection may cause a transient diarrhea or loose stools.
• Not for use in swine weighing under 300 pounds.

Pack Size

LinxMed-SP##R## (Rx)

What is LinxMed-SP^®?

An antibacterial soluble powder for the treatment of swine dysentery and for the control of necrotic enteritis in broiler chickens.
Not for use in layer and breeder chickens

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

Swine

LinxMed-SP^® Soluble Powder is indicated for the treatment of swine dysentery (bloody scours).

Broiler Chickens

LinxMed-SP^® Soluble Powder is indicated for the control of necrotic enteritis caused by Clostridium perfringens susceptible to lincomycin.

Bees

LinxMed-SP^® Soluble Powder is indicated for the control of American foulbrood (Paenibacillus larvae) in honey bees.

Benefits

• Convenient: No withdrawal time required for poultry or swine
• Highly Soluble: Dissolves readily in drinking water or to form stock solution
• Effective: Contains the proven antibiotic lincomycin hydrochloride equivalent to 400 mg lincomycin per gram
• Safe: approved by FDA

Withdrawal Period

Additional Safety Information

• Prepare fresh stock solution daily.
• May cause diarrhea and/or swelling of the anus in swine during the first two days of treatment. May cause reddening of the skin and irritable behavior in swine. Conditions are self-correcting without discontinuing treatment of lincomycin.
• The safety of lincomycin has not been demonstrated for pregnant swine or swine intended for breeding.
• Do not use the water treatment and the feed treatment simultaneously.
• Do not allow rabbits, hamsters, guinea pigs, horses, or ruminants access to water containing lincomycin.

Pack Size

MACROSYN##T## (RX)

MoxiSolv##T## Injection

What is MoxiSolv^™ Injection?

MoxiSolv Injection (moxidectin) is a ready-to-use, sterile solution containing 1% moxidectin. Moxidectin is an endectocide in the milbemycin chemical class which shares the distinctive mode of action characteristic of macrocyclic lactones. MoxiSolv Injection Is specially formulated to allow moxidectin to be absorbed from the site of injection and distributed internally to the areas of the body affected by endo- and/or ectoparasitism. Moxidectin binds selectively and with high affinity to glutamate-gated chloride ion channels which are critical to the function of invertebrate nerve and muscle cells. This interferes with neurotransmission resulting in paralysis and elimination of the parasite.

Indications

MoxiSolv Injection, when administered at the recommended dose level of 0.2 mg/2.2 lb (0.2 mg/kg) body weight, is effective in the treatment and control of the following internal and external parasites of cattle:

Benefits

• FDA-approved bioequivalent to Cydectin^® Injection
• Ready-to-use injectable parasiticide containing 1% moxidectin for use in beef and non-lactating dairy cattle
• Dosage: 1mL / 110 lbs bodyweight
• Long-lasting, persistent activity against key internal parasites 
• Short pre-slaughter withdrawal period as compared to other injectable dewormers (21 days) 
• Dung beetle friendly – a healthy population of dung beetles is environmentally beneficial but will also help you in your efforts to control internal and external parasites by reducing breeding environments for horn flies and exposure to gastrointestinal nematodes 
• The only moxidectin injectable product available in 500mL plastic bottle 

Withdrawal Period

Cattle must not be slaughtered for human consumption within 21 days of treatment.

Important Safety Information

This drug is not approved for use in female dairy cattle 20 months of age or older, including dry dairy cows. Use in these cattle may cause drug residues in milk and/or in calves born to these cows.
A withdrawal period has not been established for pre-ruminating calves.
Do not use in calves to be processed for veal.

Pack Size

Myco-Bac##R##

NeoMed##R## 325 (Rx)

What is NeoMed^® 325?

NeoMed^® 325 is an antibacterial water soluble powder for the treatment and control of colibacillosis in cattle, swine, sheep and goats, and for the control of mortality in growing turkeys.

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle (excluding veal calves), swine, sheep and goats. For the control of mortality associated with Escherichia coli organisms susceptible to neomycin sulfate in growing turkeys.

Benefits

• Safeguard: Approved for treatment of growing turkeys with no withdrawal period
• Versatile: Provides treatment for a wide variety of species
• Soluble: Dissolves readily in drinking water
• Convenient: Available in 100 g and 200 g packets plus space saving resealable 50 lb. bulk pails
• Safe: approved by FDA

Withdrawal Period

Additional Safety Information

• Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues.
• Not for use in liquid supplements.
• The concentration of neomycin required in medicated water must be adjusted to compensate for variation in age and weight of animal, the nature and severity of disease signs, and environmental temperature and humidity, each of which affects water consumption.
• If symptoms such as fever, depression, or going off feed develop, oral neomycin is not indicated as the sole treatment since systemic levels of neomycin are not obtained due to low absorption from the gastrointestinal tract.

Pack Size

OvaCyst##R## (Rx)

What is OvaCyst^®?

OvaCyst injection is a sterile solution containing 43 mcg/mL of gonadorelin (GnRH) and is indicated for treatment of cystic ovaries in dairy cattle and reproductive synchrony in beef and dairy cattle.

Dosage & Indications

 Features & Benefits

• Helps treat infertility due to ovarian cysts
• Improves breeding efficiency in dairy and beef cows
• No refrigeration required
• 3-month shelf life after first use
• The same formulation as Cystorelin^{® 1}

Withdrawal Period

Additional Safety Information

• Not for use in humans.
• Keep out of reach of children.
• Federal law restricts this drug to use by or on the order of a licensed veterinarian.
• Store at controlled room temperature 20°C - 25°C (68°F - 77°F).
• Discard product 3 months after first use.

Pack Size

¹Cystorelin is a registered trademark of Boehringer Ingelheim

Ovamed##T## (Rx)

Each mL of OvaMed^TM (altrenogest) Solution 0.22% contains 2.2 mg of altrenogest in an oil solution.

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

OvaMed^™ is indicated for the suppression of estrus in mares. Suppression of estrus allows for a predictable occurrence of estrus following drug withdrawal.

Benefits

• Attainment of regular cyclicity during the transition from winter anestrus to the physiological breeding season
• Management of prolonged estrus conditions
• Scheduled breeding during the physiological breeding season

Withdrawal Period

Do not use in horses intended for human consumption.

Additional Safety Information

• OvaMed^™ is readily absorbed by the skin. Skin contact must be avoided; protective gloves must be worn when handling this product.
• Pregnant women or women who suspect they are pregnant should not handle OvaMed^™.
• Contraindicated for use in mares having a previous or current history of uterine inflammation (i.e., acute, subacute, or chronic endometritis). Natural or synthetic gestagen therapy may exacerbate existing low-grade or 'smoldering' uterine inflammation into a fulminating uterine infection in some instances.
• Various synthetic progestins, including altrenogest, when administered to rats during the embryogenic stage of pregnancy at doses many fold greater than the recommended equine dose caused fetal anomalies, specifically masculinization of the female genitalia.
• For complete safety information please read label.

Pack Size

Oxytocin (Rx)

What is Oxytocin?

Oxytocin Injection is a sterile aqueous solution of highly purified oxytocic principle derived by synthesis or obtained from the posterior lobe of the pituitary gland of healthy domestic animals used for food by humans. Oxytocin Injection contains 20 USP Units of oxytocin and less than 0.4 units of presser activity per mL. Each mL of sterile solution also contains 0.9% w/v sodium chloride, 0.5% w/v chlorobutanol (as a preservative), with water for injection q.s. and pH adjusted to 3.0 to 5.0 with acetic acid.

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

Oxytocin is indicated for obstetrical use in sows, ewes, horses and cows, and milk let-down in cows and sows. Because of the specific action of oxytocin upon the uterine musculature, it is recommended as an aid in the management of the following conditions:

• To precipitate labor
• To accelerate normal parturition
• Postpartum evacuation of uterine debris
• Postoperative contraction of the uterus following a cesarean section and control of uterine hemorrhage

Oxytocin will contract the smooth muscle cells of the mammary gland to induce milk let-down if the udder is in a proper physiological state.

Benefits

• Choice of administration routes: IV, IM or SQ
• Versatile: Aids in a number of obstetrical procedures
• Multi-species: Treats ewes and sows, as well as cows and mares
• Storage: Store at controlled room temperature – refrigeration not required
• Safe: Approved by FDA

Withdrawal Period

No withdrawal period.

Additional Safety Information

• Oxytocin is a potent preparation, accordingly, it should be administered with due caution.
• For prepartum usage, full dilation of the cervix should be accomplished either naturally or through the administration of estrogen prior to oxytocin therapy.
• Do not use in dystocia due to abnormal presentation of the fetus until correction is accomplished.
• Oxytocin will not induce milk let-down unless the udder is in the proper physiological state.

Pack Size

PENAQUA SOL-G##R## (Rx)

What is PenAqua Sol-G^®?

PenAqua Sol-G^® is a water soluble antibiotic powder for drinking water.

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

For treatment of erysipelas in turkeys caused by Erysipelothrix rhusiopathiae.

Benefits

• Economical:
  • Each 0.500 B.U. package medicates 333 gallons of drinking water
  • Each 1.000 B.U. package medicates 666 gallons of drinking water
• Bilingual: Complete Spanish instructions included
• Convenient: Available in pre-measured foil pouches
• Safe: approved by FDA

Withdrawal Period

Additional Safety Information

• Prepare fresh stock solutions every 12 hours.
• All solutions in contact with galvanized metal should be changed every 3 hours.
• For best results, the treatment should be started at the first sign of infection. If improvement is not noted after 3 to 4 days of treatment, consult a poultry pathologist or veterinarian.

Pack Size

PolyCHEWS##R## + Krill

What is PolyCHEWS^® +Krill?

PolyCHEWS^® +Krill supports vitality and mobility in active and aging dogs

Indications

PolyCHEWS^® +Krill have a high concentration of glucosamine, hyaluronate, chondroitin & MSM for max joint support & lubrication.

Benefits

Our vitamin- and mineral-infused supplements are ideal for all dogs, especially active or aging dogs. No pet parent wants to see their furry four-legged friends suffer with joint or hip stiffness or an impaired immune system.

• Irresistibly tasty and easy to chew, even for young pups and geriatric older dogs
• Glucosamine, chondroitin sulfate and cetyl myristoleate help maintain joint health
• Especially helpful when young dogs are growing and older dogs struggle with mobility
• Beneficial for dogs of all ages during periods of intense activity
• Vitamins, minerals, fatty acids and fiber support immunity and digestion
• L-carnitine and alpha lipoic acid supports vitality and energy pathways
• Great tasting natural liver flavor treat that dogs love

How To Use

Administer during or after the animal has eaten to reduce incidence of gastrointestinal upset.
For use in adult dogs only.

Under 25 lbs: ½ chew daily
25 - 50 lbs: 1 chew daily
50 - 75 lbs: 2 chews daily
over 75 lbs: 3 chews daily

Pack Sizes

Polyglycan##R## (Rx)

What is Polyglycan^®?

Polyglycan^® is a patented formulation of hyaluronic acid, sodium chondroitin sulfate, and N-acetyl-D-glucosamine in a highly viscous aqueous solution for use in horses and dogs. Glucosaminoglycans are important components of extracellular tissue structures, including cartilage and synovial fluid.

Indications

Polyglycan^® is indicated for the replacement of lost or damaged synovial fluid. Polyglycan^® contains naturally occurring components of the synovia that play a central part in maintaining the homeostatic environment of the joint.

Polyglycan Formats

POLYGLYCAN

• Supplied in cartons (6 x 10mL vials)
• Refrigerated product

Each 10mL vial contains:

• Hyaluronic acid sodium salt50 mg
• Sodium chondroitin sulfate1000 mg
• N-acetyl-D-glucosamine1000 mg

Download Data Sheet Safety Sheet

POLYGLYCAN-HV

• HV = High Viscosity
• Supplied in individual carton, single syringe label-sealed in a blister tray
• 2.5 mL prefilled syringes
• Refrigerated product

Each 2.5mL prefilled syringe contains:

• Hyaluronic acid sodium salt20 mg
• Sodium chondroitin sulfate250 mg
• N-acetyl-D-glucosamine125 mg

Download Data Sheet Safety Sheet

POLYGLYCAN-SA

• SA = Single Administration or Small Animal
• Supplied in cartons (6 x 2.5mL vials)
• Refrigerated product

Each 2.5mL vial contains:

• Hyaluronic acid sodium salt12.5 mg
• Sodium chondroitin sulfate250 mg
• N-acetyl-D-glucosamine250 mg

Download Data Sheet Safety Sheet

Properties

• Glucosaminoglycans are important components of all extracellular tissue structures including cartilage and synovial fluid.
• The active components in Polyglycan show viscoelastic and polyionic properties similar in nature to synovial fluid.
• Patented 3-component formula has demonstrated characteristics beyond any of these components used individually.

Benefits

• Help replenish lost synovial fluid with naturally occurring elements
• Assists in normalization of synovial fluid viscosity
• Post-surgical lavage of the joint cavity and surfaces
• Patented formulation
• Convenient pre-filled syringe (Polyglycan^®-HV)

Consult with your veterinarian if you suspect your horse may have Osteoarthritis or other disease as the clinical signs can vary.

Polyglycan - Robert Hunt

I have continued to use Polyglycan^® as a standard postoperative parenteral treatment as well for essentially all of my orthopedics.
I have encountered no adverse effects either locally within the joint or any systemic reactions from either route of administration of Polyglycan^®.

Robert J. Hunt, DVM, MS, Diplomate
ACVS Hagyard Equine Medical Institute, Lexington, KY

Veterinarian response to a recently published study & article that raised concerns of Polyglycan^® safety if adminstered intravenously.

Polyglycan - Chris Morrow

We’ve used over 50,000 mL of Polyglycan^® in our practice giving us a high level of comfort and confidence in its applications.
To date there have been no adverse events to be reported by our clients or our practice.
Through my peer group I have not had conversations to suggest that their experience has been different. In my opinion, application of Polyglycan^® has benefitted the joint health and the overall well-being of horses that I have had the privilege to be the caregiver.

Chris Morrow, DVM
Mobile Veterinary Practice, Amarillo, TX

Veterinarian response to a recently published study & article that raised concerns of Polyglycan^® safety if adminstered intravenously.

Polyglycan - C.R. Johnson

the findings of this study do not correlate with what I have seen in 9 years of using this product in a clinical setting, and I disagree with the conclusion that Polyglycan^® may be harmful to the joint when administered IV.
Although the experimental model used in this study is the best model available for measuring changes in the joint environment using different medications, in my opinion, the model, as an acute chip fracture, does not replicate the disease process that I see in practice. Hopefully, the findings of this article will lead to new experiments & new discoveries about the processes involved with osteoarthritis.

C.R. Johnson, DVM, MS, DACVS
Equine Surgical Services, Versailles, KY

Veterinarian response to a recently published study & article that raised concerns of Polyglycan^® safety if adminstered intravenously.

Pack Sizes

Polyglycan##R##-HV (Rx)

What is Polyglycan^®-HV?

Polyglycan^®-HV is a patented formulation designed to replace lost or damaged synovial fluid. Polyglycan^®-HV contains naturally occurring components of the synovia that play a central role in maintaining the homeostatic environment of the joint.

Indications

Polyglycan^®-HV is indicated for the replacement of lost or damaged synovial fluid. Polyglycan^®-HV contains naturally occurring components of the synovia that play a central part in maintaining the homeostatic environment of the joint.

Each 2.5mL vial contains:

• Hyaluronic acid sodium........ 20mg
• Sodium chondroitin sulfate........250mg
• N-Acetyl-D-glucosamine........125mg

Benefits

• Helps replenish lost synovial fluid with naturally occurring elements
• Assists in the normalization of synovial fluid viscosity
• Post surgical lavage of joint cavity and surfaces
• Patented formulation
• Convenient pre-filled syringe

Withdrawal Period

Do not administer to animals that are to be slaughtered for use in food.

Pack Size

Polyglycan##R##-SA (Rx)

What is Polyglycan^®-SA?

Polyglycan^®-SA is a patented formulation designed to replace lost or damaged synovial fluid. Polyglycan^®-SA contains naturally occurring components of the synovia that play a central role in maintaining the homeostatic environment of the joint.

PRAZIQUANTEL INJECTION (Rx)

What is Praziquantel Injection?

Praziquantel Injection Cestocide is a clear solution containing 56.8 milligrams of praziquantel per mL which has been formulated for subcutaneous or intramuscular use in dogs and cats for removal of cestodes (tapeworms).

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

Praziquantel Injection Cestocide is indicated for the removal of the following canine and/or feline cestodes.

Dog

• Dipylidium caninum,
• Taenia pisiformis,
• Echinococcus granulosus,  and for
• the removal and control of Echinococcus multilocularis

Cat

• Taenia taeniaeformis
• Dipylidium caninum

Benefits

• Broad-spectrum cestocide for use in dogs and cats
• Effective against Echinococcus multilocularis in dogs
• Equivalent to the pioneer product, Droncit^® (praziquantel) Injectable Cestocide
• Flexibility of administration - Sub Q or IM
• Low toxicity - No toxicity demonstrated in dogs or cats at 5x dosage rates
• Safe for use in breeding and pregnant dogs and cats
• No known contraindications

Withdrawal Period

Not applicable.

Additional Safety Information

• Strict hygienic precautions should be taken when handling dogs or feces suspected of harboring E. multilocularis. Infected dogs treated for the first time with Praziquantel Injection solution and dogs treated at intervals greater than 28 days may shed eggs in the feces after treatment.
• Mild side effects in dogs during clinical trials were rare but included brief pain responses, mild vomiting and/or drowsy or staggering gait.
• Mild side effects in cats during clinical trials were rare but included diarrhea, weakness, vomition, salivation, sleepiness, burning on injection and/or temporary lack of appetite.
• Local irritation or swelling at the site of subcutaneous injection has been reported for cats.

Pack Size

Pro-Bac##T## Vaccines

PRO-PEN-G##R##(RX)

What is Pro-Pen-G^®?

Penicillin G Procaine Injectable Suspension is available in 100 mL, 250 mL and 500 mL multiple-dose vials. Each mL contains: Active Ingredients: Penicillin G potassium 300,000 units*, Procaine hydrochloride 130.8 mg*. Inactive Ingredients: Methylparaben 1.3 mg, Propylparaben 0.2 mg, Sodium citrate 10 mg, Sodium carboxymethylcellulose 1 mg, Povidone 5 mg, Lecithin 6 mg, Sodium formaldehyde sulfoxylate 0.2 mg, Procaine hydrochloride 20 mg, and Water for Injection, q.s
*Penicillin G potassium and Procaine hydrochloride react to form penicillin G procaine.

CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian

Indications

Cattle

For the treatment of:

• bacterial pneumonia (shipping fever) caused by Pasteurella multocida

Sheep

For the treatment of:

• bacterial pneumonia (shipping fever) caused by Pasteurella multocida

Swine

For the treatment of:

• erysipelas caused by Erysipelothrix rhusiopathiae

Horses

For the treatment of:

• strangles caused by Streptococcus equi.

Benefits

• Versatile: Treats a variety of infections in a number of species
• Proven effective: Millions of doses delivered worldwide
• Fast acting: Noticeable improvement within 36 to 48 hours
• Safe: Approved by FDA

Withdrawal Period

Additional Safety Information

• Sensitivity reactions to penicillin, such as hives or respiratory distress, may occur in some animals. If respiratory distress is severe, immediate injection of epinephrine or antihistamine may be necessary.
• Use of this drug may result in overgrowth of non-susceptible organisms, including fungi.

Pack Size

ProstaMate##R## (Rx)

What is ProstaMate^®?

ProstaMate is a sterile solution that contains 5 mg/mL of dinoprost—a naturally occuring prostaglandin F₂-alpha — and is indicated for use in cattle.

Dosage & Indications

ProstaMate Sterile Solution is indicated as a luteolytic agent. ProstaMate is effective only in those cattle having a corpus luteum, i.e., those which ovulated at least five days prior to treatment.

 Features & Benefits

• A thoroughly researched molecule you can trust for safety & performance
• No meat or milk withdrawal
• A synchronized breeding program with ProstaMate can:
  • Improve pregnancy rates
  • Reduce time necessary for heat detection
• The same formulation as Lutalyse^{® 3}

Withdrawal Period

Additional Safety Information

• Not for use in humans.
• Women of childbearing age, asthmatics, and persons with bronchial and other respiratory problems should exercise extreme caution when handling this product.
• Accidental spillage on the skin should be washed off immediately with soap and water.
• No vial stopper should be entered more than 20 times. For this reason, the 90 mL bottle should only be used for cattle. 
• Nonsteroidal anti-inflammatory drugs may inhibit prostaglandin synthesis; therefore this class of drugs should not be administered concurrently.
• Store at controlled room temperature 20° - 25°C (68° - 77°F). Protect from freezing.
• Severe localized clostridial infections associated with injection of dinoprost tromethamine have been reported

Pack Size

SMZ-Med##R## 454 (Rx)

What is SMZ-Med^® 454?

SMZ-Med^® 454 is a soluble powder available in a 453.5 g foil pack that contains 100% sodium sulfamethazine.

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

For the control and treatment of the following diseases when caused by one or more of the following pathogenic organisms susceptible to sulfamethazine.

Cattle

For the treatment of:

• Bacterial Pneumonia and Bovine Respiratory Disease Complex (Shipping Fever Complex) (Pasteurella spp.)
• Colibacillosis (Bacterial Scours) (Escherichia coli)
• Necrotic Pododermatitis (Foot Rot) (Fusobacterium necrophorum)
• Calf Diphtheria (Fusobacterium necrophorum)
• Acute Metritis (Streptococcus spp.)

Beef Cattle

For the treatment of:

• Acute Mastitis (Streptococcus spp.)

Swine

For the treatment of:

• Porcine Colibacillosis (Bacterial Scours) (Escherichia coli)
• Bacterial Pneumonia (Pasteurella spp.)

Chickens

For the control of:

• Infectious Coryza (Avibacterium paragallinarum)
• Coccidiosis (Eimeria tenella, Eimeria necatrix)
• Acute Fowl Cholera (Pasteurella multocida)
• Pullorum Disease (Salmonella Pullorum)

Turkeys

For the control of:

• Coccidiosis (Eimeria meleagrimitis, Eimeria adenoeides)

Benefits

• Highly Soluble: Mixes readily and thoroughly in water
• Convenient: Once-a-day dosage in drinking water or as a drench
• Fast Acting: Symptom relief usually apparent in two to three days
• Easy to Use: One packet/gallon of water prepares recommended 12.0% stock solution
• Safe: Approved by FDA

Withdrawal Period

Additional Safety Information

• Have only medicated water available during treatment. Ensure adequate drug dosage and water intake.
• Cattle and calves not drinking or eating must be dosed by drench or with immediate sulfamethazine bolus.
• For best results, treat animals individually.
• Excessive dosage may cause toxic reactions.
• Hatchability of eggs laid during medication with sulfas, and for short periods thereafter, may be adversely affected.

Pack Size

SPECLINX-50##R## (Rx)

What is SpecLinx-50^®?

SpecLinx-50^® is a water soluble antibacterial and antimycoplasmal powder for use in chickens.

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

For use in chickens up to 7 days of age as an aid in the control of: Airsacculitis caused by either Mycoplasma synoviae or Mycoplasma gallisepticum susceptible to lincomycin-spectinomycin. Complicated Chronic Respiratory Disease (Air Sac Infection) caused by Escherichia coli and M. gallisepticum susceptible to lincomycin-spectinomycin.

75 g packet contains:

Benefits

• Highly soluble: Mixes easily and completely in water
• Convenient: Pre-measured packaging provides for handy on-site mixing
• Stable: Stores well at room temperature
• Bilingual: Complete Spanish instructions included
• FDA approved

Withdrawal Period

No withdrawal period.

Additional Safety Information

• Discard medicated drinking water daily and replace with fresh medicated drinking water.

Pack Size

SpectoGard##R## Scour-Chek##R##(RX)

What is SpectoGard^® Scour-Chek^®

SpectoGard^® Scour-Chek^® is an oral solution intended as an anti-infective for young pigs. Each mL contains spectinomycin dihydrochloride pentahydrate equivalent to 50 mg of spectinomycin activity

CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

For use in pigs under four (4) weeks of age for treatment and control of porcine enteric colibacillosis (scours) caused by E. coli susceptible to spectinomycin.

Benefits

• Effective
  Proven spectinomycin activity
• Convenient
  No mixing, ready-to-use
• Palatable
  Readily accepted
• Fast acting
  Positive results in 3 to 5 days
• Safe
  Approved by FDA

Withdrawal Period

Pack Sizes

SpectoGard##R## Sterile Solution (RX)

Mannheimia haemolytica

Pasteurella multocida

Histophilus somni

SPECTOGARD##R## WSP (Rx)

What is SpectoGard^® Water Soluble Powder?

SpectoGard^® is a water soluble powder intended as an anti-infective for growing chickens.

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

SpectoGard^® is indicated as an aid in the prevention or control of losses due to chronic respiratory disease (CRD) associated with Mycoplasma gallisepticum (PPLO) and infectious synovitis associated with Mycoplasma synoviae.

Each 1000 g contains:
Spectinomycin dihydrochloride pentahydrate equivalent to spectinomycin activity ...... 500.00 g

Benefits

• Highly Soluble
  Mixes readily and thoroughly in water
• Stable
  Effective over extended periods
• Versatile
  Approved for chronic respiratory disease and infectious synovitis
• Easy to Use
  Suitable for use in automatic water proportioners
• Safe
  Approved by FDA

Withdrawal Period

Additional Safety Information

• Rarely some individuals who handle spectinomycin develop serious reactions involving skin, nails and eyes. Individuals who have experienced rash or other evidence of allergic reaction should avoid further contact with spectinomycin.
• As an aid in the prevention and control of losses due to CRD associated with M. gallisepticum, provide only medicated drinking water for the first 3 days of life and for one day following each vaccination.
• As an aid in controlling infectious synovitis due to Mycoplasma synoviae in broiler chickens, provide only medicated drinking water for the first 3 – 5 days of life.

Pack Size

Stimulator##R## Vaccines

SulfaMed##R##(RX)

What is SulfaMed^®?

SulfaMed^® (sulfadimethoxine) Injection 40% is a low-dosage, rapidly absorbed, long-acting sulfonamide, effective for the treatment of shipping fever complex, bacterial pneumonia, calf diphtheria, and foot rot in cattle.

CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

For the treatment of bovine respiratory disease complex (shipping fever complex) and bacterial pneumonia associated with Pasteurella spp. sensitive to sulfadimethoxine; necrotic pododermatitis (foot rot) and calf diptheria caused by Fusobacterium necrophorum sensitive to sulfadimethoxine.

Benefits

• Broad-spectrum antibacterial activity
• Convenient, once-a-day dosing
• Rapid therapeutic blood levels
• Sustained therapeutic blood levels
• Safe: Approved by FDA

Withdrawal Period

Additional Safety Information

• During treatment period, make certain animals maintain adequate water intake.
• Tissue damage may result from perivascular infiltration.
• The usual cautions in sulfonamide therapy should be observed.

Pack Size

SUSTAIN III##R## CALF BOLUS (RX)

What is Sustain III^® Calf Bolus?

SUSTAIN III^® Boluses (Sulfamethazine Sustained Release Boluses) are intended for oral administration to ruminating replacement calves (calves over one (1) month old that are not on an all-milk diet).

CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

Sustain III^® Calf Boluses are indicated for the treatment of the following diseases when caused by one or more of the following pathogenic organisms sensitive to sulfamethazine: Bacterial Pneumonia (Pasteurella spp.), Colibacillosis (Bacterial Scours) (E. coli) and Calf Diphtheria (Fusobacterium necrophorum).

Benefits

• Less handling
  72 hours of sustained antibacterial activity
• Effective
  Broad spectrum activity against a variety of common calf diseases
• Ideal for receiving programs
  Helps beat infections early
• Fast acting
  Achieves therapeutic blood levels in six hours
• Safe
  Approved by FDA

Withdrawal Period

Additional Safety Information

• This drug may cause toxic reactions and irreparable injury unless administered with adequate and continuous supervision. Follow recommended dosages carefully.
• Fluid intake must be adequate at all times during the three-day therapy.

Pack Size

SUSTAIN III##R## CATTLE BOLUS (RX)

What is Sustain III^® Cattle Bolus?

SUSTAIN III^® Boluses (Sulfamethazine Sustained Release Boluses) are intended for oral administration to beef cattle and non-lactating dairy cattle.

CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

SUSTAIN III^® Cattle Boluses are indicated for the treatment of the following diseases when caused by one or more of the following pathogenic organisms sensitive to sulfamethazine: Bacterial Pneumonia and Bovine Respiratory Disease Complex (Shipping Fever Complex) (Pasteurella spp.), Colibacillosis (Bacterial Scours) (E. coli), Necrotic Pododermatitis (Foot Rot), Calf Diphtheria (Fusobacterium necrophorum), Acute Metritis (Streptococcus spp.).

Benefits

• Less handling
  72 hours of sustained antibacterial activity
• Effective
  Broad spectrum activity against a variety of common cattle diseases
• Ideal for receiving programs
  Helps beat infections early
• Fast acting
  Achieves therapeutic blood levels in six hours
• Safe
  Approved by FDA

Withdrawal Period

Additional Safety Information

• This drug may cause toxic reactions and irreparable injury unless administered with adequate and continuous supervision. Follow recommended dosages carefully.
• Fluid intake must be adequate at all times during the three-day therapy.

Pack Size

Tandem##T## Oral

What is Tandem^™ Oral?

Tandem^™ Oral is a joint supplement that can be used in:

• Young and developing horses
• To support joint health during training and competition
• To help maintain mobility in senior horses

Indications

The combination of hyaluronic acid, chondroitin sulfate, glucosamine and methysulfonylmethane (MSM) help maintain joint health and mobility in horses. May be used in conjunction with Polyglycan Sterile Solution to support the joint function.

Benefits

• Helps maintain joint health in young and developing horses, as well as senior horses
• Supports joint health during training and competition
• Use in conjunction with Polyglycan^® Sterile Solution to support the joint function
• Granules which can be sprinkled on food or given directly

Withdrawal Period

No withdrawal period.

Pack Size

TETRAMED##R## 324 HCA (Rx)

What is TetraMed^® 324 HCA?

TetraMed^® 324 HCA is a versatile antibiotic used to treat many different bacterial infections.

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

For use in the control and treatment of the following conditions in swine, calves and poultry.

Swine

Use for the control and treatment of:

• bacterial enteritis (scours) caused by Escherichia coli;
• bacterial pneumonia associated with Actinobacillus pleuropneumoniae, Pasteurella spp. and Klebsiella spp. sensitive to tetracycline hydrochloride

Calves

Use for the control and treatment of:

• bacterial enteritis (scours) caused by Escherichia coli;
• bacterial pneumonia associated with Actinobacillus pleuropneumoniae, Pasteurella spp. and Klebsiella spp. sensitive to tetracycline hydrochloride

Chickens

For the control of:

• chronic respiratory disease (CRD) and air sac disease caused by Mycoplasma gallisepticum and Escherichia coli;
• infectious synovitis caused by Mycoplasma synoviae sensitive to tetracycline hydrochloride

Turkeys

For the control of:

• infectious synovitis caused by Mycoplasma synoviae;
• bluecomb (transmissible enteritis, coronaviral enteritis) complicated by organisms sensitive to tetracycline hydrochloride

Benefits

• Versatile
  Safe, effective treatment for a variety of species
• Broad Spectrum
  Treats and controls a number of common diseases
• Proven
  Tetracycline hydrochloride has been demonstrated effective on millions of animals
• High Citric Acid (HCA) Content
  Clearer, more soluble, stays in solution longer

Withdrawal Period

Additional Safety Information

• When used in plastic or stainless steel waterers, prepare fresh solution every 24 hours.
• When used in galvanized waterers or automatic medicators, prepare fresh solution every 12 hours.
• Prepare fresh stock solution every 12 hours.
• Use as the sole source of tetracycline.
• Special directions for baby calves and baby pigs: administer this product one hour before or two hours after feeding with milk or milk replacers. Provide clean (unmedicated) water at all times.

Pack Size

Tetroxy##R## 25 (Rx)

What is Tetroxy^® 25?

A broad spectrum antibiotic for the control and treatment of specific diseases in poultry, cattle, sheep and swine and honey bees.

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

For control and treatment of specific diseases in poultry, cattle, sheep, swine, and honey bees.

Chickens

For control and treatment of:

• Infectious synovitis caused by Mycoplasma synoviae
• Chronic respiratory disease (CRD) and air sac infection caused by Mycoplasma gallisepticum and Escherichia coli
• Fowl cholera caused by Pasteurella multocida

Turkeys

For control and treatment of:

• Hexamitiasis caused by Hexamita meleagridis
• Infectious synovitis caused by Mycoplasma synoviae
• Growing Turkeys–Complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis)

Swine

For control and treatment of:

• Bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis.
• Bacterial pneumonia (shipping fever complex) caused by Pasteurella multocida.
• For Breeding Swine: Leptospirosis (reducing the incidence of abortions and shedding of leptospira) caused by Leptospira pomona.

Calves, Beef Cattle and Non‑lactating Dairy Cattle

For control and treatment of:

• Bacterial enteritis caused by Escherichia coli.
• Bacterial pneumonia (shipping fever complex) caused by Pasteurella multocida.

Sheep

For control and treatment of:

• Bacterial enteritis caused by Escherichia coli.
• Bacterial pneumonia (shipping fever complex) caused by Pasteurella multocida.

Bees

For control and treatment of:

• For control of American Foulbrood caused by Paenibacillus larvae
  CONTRAINDICATION: Dusting of uncapped brood cells has been reported to cause death of larval honey bees. Do not dust uncapped brood cells.

Benefits

• Versatile: Approved for use in multiple food animal species
• Broad spectrum: Treats and controls a variety of disease organisms
• Short withdrawal time: Only five days after the last administration
• Oral dosage form: Reduces handling and animal stress
• Soluble: Readily dissolves in water
• Safe: Approved by FDA

Withdrawal Period

Additional Safety Information

• Use as the sole source of oxytetracycline.
• Prepare fresh solutions every 24 hours.
• The concentration of drug required in medicated water must be adequate to compensate for variation in the age of the animal, feed consumption rate and environmental temperature and humidity, each of which affects water consumption.

Pack Size

TETROXY##R## 343 (Rx)

What is Tetroxy^® 343?

Tertroxy^® 343 is a broad spectrum antibiotic soluble powder, containing 343g oxytetracycline HCI per pound.

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

Tetroxy^® 343 Soluble Powder is indicated for the control and treatment of:

 

Calves, Beef Cattle, Non-Lactating Dairy Cattle

bacterial enteritis caused by Escherichia coli. Bacterial pneumonia (shipping fever complex) caused by Pasteurella multocida.

 

Swine

bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis. Bacterial pneumonia caused by Pasteurella multocida.

For Breeding Swine

Leptospirosis caused by Leptospira pomona.

 

Sheep

bacterial enteritis caused by Escherichia coli. Bacterial pneumonia (shipping fever complex) caused by Pasteurella multocida.

 

Chickens

infectious synovitis caused by Mycoplasma synoviae. Chronic respiratory disease (CRD) and air sac infection caused by Mycoplasma gallisepticum and Escherichia coli. Fowl cholera caused by Pasteurella multocida.

 

Turkeys

hexamitiasis caused by Hexamita meleagridis. Infectious synovitis caused by Mycoplasma synoviae.
GROWING TURKEYS - Complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis).

 

Honey Bees

American Foulbrood caused by Paenibacillus larvae.

 

Fish

skeletal tissues in finfish fry and fingerlings as an aid in identification.

Benefits

• Approved for use in multiple food animal species
• Controls a variety of disease organisms
• Short withdrawal time: Only five days after the last administration in turkeys, cattle or sheep & zero slaughter withdrawal in swine.
• Oral dosage reduces handling and animal stress
• Soluble: Readily dissolves in water
• Approved by FDA

Withdrawal Periods

Additional Safety Information

• Not for use in liquid feed supplements.
• Dusting of uncapped brood cells has been reported to cause death of larval honey bees. Do not dust uncapped brood cells.
• Prepare fresh solutions every 24 hours
• For treatment of fish: Oxytetracycline hydrochloride will acidify the water. The pH should be maintained at an acceptable level for fish by the addition of a buffer. Monitor water quality and temperature.
• Do not discharge marking immersion water containing oxytetracycline into surface waters.
• Administer 1 hour before or 2 hours after feeding milk or milk replacers.

Pack Sizes

Tetroxy##R## HCA-1400 (Rx)

What is Tetroxy^® HCA-1400?

Tetroxy^® HCA-1400 is a water soluble antibiotic powder for the control and treatment of specific diseases in chickens, turkeys and swine.

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

For use in the drinking water of poultry and swine as a control of specific diseases susceptible to oxytetracycline.

Chickens

For control of:

• Control of infectious synovitis caused by Mycoplasma synoviae, susceptible to oxytetracycline.
• Control of chronic respiratory disease (CRD) and air sac infections caused by Mycoplasma gallisepticum and Escherichia coli, susceptible to oxytetracycline.
• Control of fowl cholera caused by Pasteurella multocida, susceptible to oxytetracycline.

Turkeys

For control of:

• Control of hexamitiasis caused by Hexamita meleagridis, susceptible to oxytetracycline.
• Control of infectious synovitis caused by Mycoplasma synoviae, susceptible to oxytetracycline.
• Growing Turkeys: Control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis), susceptible to oxytetracycline.

Swine

For control of:

• Bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis, susceptible to oxytetracycline.
• Bacterial pneumonia caused by Pasteurella multocida, susceptible to oxytetracycline.
• For Breeding Swine: Leptospirosis (reducing the incidence of abortions and shedding of leptospira) caused by Leptospira pomona, susceptible to oxytetracycline.

Benefits

• Versatile
  Antibiotic treatment for chickens, turkeys and swine
• Convenient
  Zero withdrawal time before slaughter
• Economical
  Full range of packaging options for the way producers work today
• Soluble
  Readily dissolves in water
• Safe
  Approved by FDA

Withdrawal Period

Additional Safety Information

• Not for use in liquid Type B Medicated Feeds.
• Use as the sole source of oxytetracycline.
• Not to be used for more than 14 consecutive days in chickens and turkeys.
• Not to be used for more than 5 consecutive days in swine.

Pack Size

Tetroxy##R## HCA-1772 (Rx)

What is Tetroxy^® HCA-1772?

Tetroxy^® HCA-1772 is a water soluble antibiotic powder for control and treatment of specific diseases in swine

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

For use in the drinking water of swine. For the control and treatment of the following diseases:

Swine

• Bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis, susceptible to oxytetracycline.
• Bacterial pneumonia caused by Pasteurella multocida, susceptible to oxytetracycline.

For Breeding Swine

• Leptospirosis (reducing the incidence of abortions and shedding leptospira) caused by Leptospira pomona, susceptible to oxytetracycline.

Benefits

• Broad spectrum: Economical treatment for a variety of common swine diseases
• Convenient: Zero withdrawal time before slaughter
• Soluble: Readily dissolves in water
• Safe: Approved by FDA

Withdrawal Period

Additional Safety Information

• Not for use in liquid Type B Medicated Feeds.
• Use as the sole source of oxytetracycline.
• Not to be used for more than 5 consecutive days.

Pack Size

Tetroxy##R## HCA-280 (Rx)

What is Tetroxy^® HCA-280?

Tetroxy^® HCA-280 is a water soluble antibiotic powder for the control and treatment of specific diseases in chickens, turkeys and swine.

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

For use in the drinking water of poultry and swine as a control of specific diseases susceptible to oxytetracycline.

Chickens

For control of:

• Control of infectious synovitis caused by Mycoplasma synoviae, susceptible to oxytetracycline.
• Control of chronic respiratory disease (CRD) and air sac infections caused by Mycoplasma gallisepticum and Escherichia coli, susceptible to oxytetracycline.
• Control of fowl cholera caused by Pasteurella multocida, susceptible to oxytetracycline.

Turkeys

For control of:

• Control of hexamitiasis caused by Hexamita meleagridis, susceptible to oxytetracycline.
• Control of infectious synovitis caused by Mycoplasma synoviae, susceptible to oxytetracycline.
• Growing Turkeys: Control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis), susceptible to oxytetracycline.

Swine

For control of:

• Bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis, susceptible to oxytetracycline.
• Bacterial pneumonia caused by Pasteurella multocida, susceptible to oxytetracycline.
• For Breeding Swine: Leptospirosis (reducing the incidence of abortions and shedding of leptospira) caused by Leptospira pomona, susceptible to oxytetracycline.

Benefits

• Versatile
  Antibiotic treatment for chickens, turkeys and swine
• Convenient
  Zero withdrawal time before slaughter
• Economical
  Full range of packaging options for the way producers work today
• Soluble
  Readily dissolves in water
• Safe
  Approved by FDA

Withdrawal Period

Additional Safety Information

• Not for use in liquid Type B Medicated Feeds.
• Use as the sole source of oxytetracycline.
• Not to be used for more than 14 consecutive days in chickens and turkeys.
• Not to be used for more than 5 consecutive days in swine.

Pack Size

Viceton##R## Tablets (Rx)

What is Viceton^® Tablets?

Viceton® is a broad-spectrum antibiotic, indicated for use in dogs.

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

Viceton^® is a broad-spectrum antibiotic, indicated for the following conditions in dogs:

• Bacterial pulmonary infections caused by Staphylococcus aureus, Streptococcus pyogenes and Brucella bronchiseptica
• Infections of the urinary tract caused by Escherichia coli, Proteus vulgaris, Corynebacterium renale, Streptococcus spp. and hemolytic Staphylococcus
• Enteritis caused by E. coli, Proteus spp., Salmonella spp., and Pseudomonas spp.
• Infections associated with canine distemper caused by B. bronchiseptica, E. coli, P. aeruginosa, Proteus spp., Shigella spp. and Neisseria catarrhalis.

Benefits

• Fast
  Diffuses readily into all body tissues and fluids. Reaches infected tissue very rapidly
• Easy to administer
  Tablets are small, scored, and coated for easy pilling
• Effective
  
  • Provides rapid clinical response against a wide range of pathogens
  • Most susceptible infectious disease organisms will respond to chloramphenicol therapy in three to five days
  • Reaches significant concentrations in the aqueous and vitreous humors of the eye and has marked ability to diffuse into the cerebrospinal fluid
• Low resistance
  Resistance is rare compared with other antibiotics.
• Safe
  Approved by FDA

Withdrawal Period

Not applicable

Additional Safety Information

• Not for use in animals which are raised for food production.
• Do not administer simultaneously with penicillin or streptomycin.
• Do not administer in conjunction with or two hours prior to the induction of general anesthesia with pentobarbital.
• Do not administer to dogs maintained for breeding purposes.
• May depress hematopoietic activity in the bone marrow.

Pack Size

XYLAMED##T## (Rx)

What is XylaMed^TM?

XylaMed^TM is a sedative and analgesic for use in horses and cervidae only

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Indications

XylaMed^TM should be used in horses and Cervidae (Fallow Deer, Mule Deer, Sika Deer, White-Tailed Deer and Elk) when it is desirable to produce a state of sedation accompanied by a shorter period of analgesia.

Benefits

• Sedation
  Facilitates the handling of aggressive or nervous animals, reducing physical stress and risk to both animal and practitioner
• Successfully used in conducting diagnostic procedures, Orthopedic procedures, Dental procedures & minor surgical procedures of short duration
• Therapeutic medication for relief of pain following injury or surgery
• Preanesthetic to general anaesthesia or in conjunction with local anesthetics during major surgical procedures
• Safe
  approved by FDA

Additional Safety Information

• This drug should not be administered to domestic food-producing animals.
• Not for use in horses intended for human consumption.
• Careful consideration should be given before administering to horses or Cervidae with significantly depressed respiration, severe pathologic heart disease, advanced liver or kidney disease, severe endotoxic or traumatic shock, or stress conditions such as extreme heat, cold, high altitude or fatigue.
• Do not use during the breeding season of Cervidae.
• Do not use in conjunction with tranquilizers.
• Intracarotid arterial injection should be avoided.
• Withdrawal Period – Delete this section, it’s not applicable.

Pack Size