Each milliliter of Banamine Transdermal pour-on contains 50 mg flunixin (equivalent to 83 mg flunixin meglumine), 150 mg pyrrolidone, 50 mg L-menthol, 500 mg propylene glycol dicaprylate/dicaprate NF, 0.20 mg FD&C Red No. 40, and glycerol monocaprylate NF qs.
Pain and fever can cause cattle to go off feed. But now, easy-to-use Banamine Transdermal® (flunixin transdermal solution) helps get ‘em back where they belong. FDA-approved to control pain due to foot rot and fever due to BRD, Banamine Transdermal is the only non-steroidal anti-inflammatory (NSAID) cattle product available with a convenient pour-on route of administration.
Banamine Transdermal pour-on is indicated for the control of fever associated with bovine respiratory disease and the control of pain associated with foot rot in beef cattle, and in dairy heifers less than 20 months of age. Each ml of Banamine Transdermal pour-on contains 50 mg flunixin. Apply one dose of 3 ml per 100 lbs. topically in a narrow strip along the back from the withers to the tailhead. Do not treat cattle if the hide is wet or may get wet within 6 hours. Not for use in beef bulls intended for breeding; dairy bulls; female dairy cattle 20 months of age or older, including dry dairy cows; and suckling beef calves, dairy calves, and veal calves. Flunixin transdermal solution.
Banamine Transdermal pour-on is indicated for the control of pyrexia associated with bovine respiratory disease and the control of pain associated with foot rot in steers, beef heifers, beef cows, beef bulls intended for slaughter, and replacement dairy heifers under 20 months of age.
Features of Banamine Transdermal For Cattle
- FDA approved pour on for pain control.
- Easy to dose.
Specifications of Banamine Transdermal For Cattle
- Keep out of reach of children.
- Only for topical use in beef and dairy cattle.
- Do not use Banamine Transdermal pour-on within 48 hours of expected parturition.
- Do not use in animals showing hypersensitivity to ﬂunixin meglumine.
- Cattle must not be slaughtered for human consumption within 8 days of the last treatment.
- Not 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 or heifers.
- Not for use in suckling beef calves, dairy calves, and veal calves. A withdrawal period has not been established for this product in pre-ruminating calves.
- Not for use in dairy or beef bulls intended for breeding because reproductive safety has not been evaluated.
Dosage and Administration
Apply only once at a dose of 3.3 mg flunixin per kg body weight (1.5 mg/lb; 3 mL per 100 lbs) topically in a narrow strip along the dorsal midline from the withers to the tailhead. Round all doses up to the nearest weight increment on the dosing chamber. Do not treat cattle if the hide is wet or may get wet in the six hours after dosing because effectiveness has not been evaluated under wet hide conditions. Practice the Administration and Overfill Reduction Instructions a few times to become familiar with operating the package before dosing animals.
As a class, cyclo-oxygenase inhibitory NSAIDs may be associated with gastrointestinal, renal, and hepatic toxicity. Sensitivity to drug-associated adverse events varies with the individual patient. Patients at greatest risk for adverse events are those that are dehydrated, on concomitant diuretic therapy, or those with renal, cardiovascular, and/or hepatic dysfunction. Banamine transdermal should be used with caution in animals with suspected pre-existing gastric erosions or ulcerations. Concurrent administration of other NSAIDs, corticosteroids, or potentially nephrotoxic drugs should be avoided or used only with careful monitoring because of the potential increase of adverse events.
NSAIDs are known to have potential effects on both parturition (see Contraindications) and the estrous cycle. There may be a delay in the onset of estrus if flunixin is administered during the prostaglandin phase of the estrous cycle. NSAIDs are known to have the potential to delay parturition through a tocolytic effect. The use of NSAIDs in the immediate post-partum period may interfere with uterine involution and expulsion of fetal membranes. Cows should be monitored carefully for placental retention and metritis if Banamine Transdermal pour-on is used within 24 hours after parturition. Not for use in dairy or beef bulls intended for breeding because reproductive safety has not been evaluated.
Prices of Banamine Transdermal For Cattle
$60.79 – $218.45