Qualifying purchases: Purchases must be made from September 1, 2022 through April 1, 2023 with valid dated invoices. Qualifying purchases have to exceed $2,000 per upload of invoices. Each individual invoice may be below $2,000 providing that the total amount of Virbac products on the uploaded invoices exceeds this amount.
Invoices must be uploaded on our website on or before April 1, 2023. Customers can participate in the offer more than once but rewards are capped at 5 vests per customer, corresponding to a qualifying purchase of $10,000.
Eligibility: Cattle producers that are US residents and Veterinary Clinics are eligible to participate. This offer is limited to 5 vests maximum per customer.
*Qualifying Virbac products are Tulissin® 100 (tulathromycin injection) vials of 50 mL, 100 mL, 250 mL and 500 mL; Tenotry™ (enrofloxacin) injectable solution, vials of 100 mL, 250 mL and 500 mL
Legal info: ©2023 Virbac Corporation. All Rights Reserved.
TULISSIN® is a registered trademark of Virbac S.A. TENOTRYL is a trademark of Virbac S.A.
Important Safety Information
IMPORTANT SAFETY INFORMATION
TULISSIN® 100 (tulathromycin injection): Not for use in humans. Ensure a pre-slaughter withdrawal time of eighteen (18) days in cattle and five (5) days in swine. Do not use in 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. The effects of tulathromycin on bovine and swine reproductive performance, pregnancy and lactation have not been determined. Do not use in animals known to be hypersensitive to the product.
IMPORTANT SAFETY INFORMATION
TULISSIN® 25 (tulathromycin injection): Not for use in ruminating cattle. Ensure a pre-slaughter withdrawal time of twenty-two (22) days in calves and five (5) days in swine. The effects of tulathromycin on bovine and swine reproductive performance, pregnancy and lactation have not been determined. Do not use in animals known to be hypersensitive to the product.
SWINE IMPORTANT SAFETY INFORMATION
Tenotryl™ (enrofloxacin) 100 mg/ml Antimicrobial Injectable Solution: Not for use in humans. For intramuscular or subcutaneous use in swine. Federal (USA) law restricts this drug to use by or on the order of a licensed veterinarian and prohibits the extra-label use of this drug in food producing animals. To assure responsible antimicrobial drug use, enrofloxacin should only be used as a second-line drug for colibacillosis in swine following consideration of other therapeutic options. Animals intended for human consumption must not be slaughtered within 5 days of receiving a single injection dose. The effects of enrofloxacin on swine reproductive performance, pregnancy and lactation have not been adequately determined. The long-term effects on articular joint cartilage have not been determined in pigs above market weight. Subcutaneous or intramuscular injection in swine can cause a transient local tissue reaction and may result in trim loss of edible tissue at slaughter. Quinolone-class drugs should be used with caution in animals with known or suspected Central Nervous System (CNS) disorders.
CATTLE IMPORTANT SAFETY INFORMATION
Tenotryl™ (enrofloxacin) 100 mg/ml Antimicrobial Injectable Solution: Not for use in humans. For subcutaneous use in beef cattle and non-lactating dairy cattle. Not for use in female dairy cattle 20 months of age or older or in calves to be processed for veal. Federal (USA) law restricts this drug to use by or on the order of a licensed veterinarian and prohibits the extra-label use of this drug in food producing animals. Animals intended for human consumption must not be slaughtered within 28 days from the last treatment. This product 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 the calves born to these cows. A withdrawal period has not been established for this product in pre-ruminating calves. The effects of enrofloxicin on cattle reproductive performance, pregnancy and lactation have not been adequately determined. Do not exceed a 20 mL dose per injection site. Subcutaneous injection in cattle can cause a transient local tissue reaction and may result in trim loss of edible tissue at slaughter. Quinolone-class drugs should be used with caution in animals with known or suspected Central Nervous System (CNS) disorders.
IMPORTANT SAFETY INFORMATION
TIA™ 12.5% (tiamulin hydrogen fumarate) liquid concentrate: Not for use in humans - for use in drinking water of swine only. Withdraw medicated water 3 days before slaughter after treatment at 3.5mg per pound body weight and 7 days before slaughter after treatment at 10.5mg per pound body weight. Prepare fresh medicated water daily. Use as the only source of drinking water for 5 days. Do not use undiluted. The effects of tiamulin on swine reproductive performance, pregnancy and lactation have not been determined. Swine being treated with TIA 12.5% liquid concentrate should not have access to feeds containing polyether ionophores (e.g., monensin, lasalocid, narasin, salinomycin and semduramicin) as adverse reactions may occur. In rare cases, redness of the skin primarily over the ham and underline has been observed during medication. If these signs appear, discontinue use of this drug.