Label: CATTLYST- laidlomycin propionate potassium granule
- NDC Code(s): 54771-2000-1
- Packager: Zoetis Inc.
- Category: OTC TYPE A MEDICATED ARTICLE ANIMAL DRUG LABEL
Drug Label Information
Updated September 2, 2022
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Mixing And Feeding Instructions
Read all directions carefully before mixing and feeding.
DO NOT FEED UNDILUTED
Type B Medicated Feed
Thoroughly mix the following amounts of Cattlyst 50G to make one ton of Type B Medicated Feed to provide the concentrations shown in TABLE 1. With low use levels of Cattlyst 50G (e.g. two lb/ton or less), the use of an intermediate blending step should be performed to ensure adequate mixing.
Liquid feeds made with Cattlyst 50G shall have a dry matter content in the range of 62%-75%, pH in the range of 6.0-8.0 and drug level of 100-2000 g/ton. Its label shall carry daily and prior to use recirculating/agitation directions and an expiration of 21 days from date of manufacture. The Type C feed made with this Type B liquid feed shall be fed within seven days from date of manufacture.
TABLE 1 - Type B Medicated Feed Pounds of Cattlyst 50G per ton of supplement Laidlomycin Concentration in Type B Medicated Feed (Grams per ton) 2.0 100 4.0 200 20.0 1000 40.0 2000 Type C Medicated Feed
Thoroughly mix the following amounts of Cattlyst 50G to make one ton of Type C Medicated Feed that provides 5-10 grams of laidlomycin propionate potassium per ton of feed on a 90% dry matter basis (TABLE 2). An intermediate blending step should be performed to ensure adequate mixing. For example, use one part Cattlyst 50G Type A Medicated Article with nine parts of feed ingredients to prepare an intermediate blend before preparing a Type C Medicated Feed. Feed continuously in the range of 5-10 grams per ton to growing and finishing beef cattle.
TABLE 2 - Type C Medicated Feed Pounds of Cattlyst 50G per ton of complete feed Pounds of a 1,000 g/ton Type B Medicated Feed per ton of complete feed Laidlomycin Concentration in complete Type C feed 90% dry matter basis (grams per ton) 0.1 10 5 0.15 15 7.5 0.20 20 10 - Caution
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WARNING
When mixing and handling Cattlyst 50G use appropriate protective clothing, eye, face, and respiratory protection. If accidental eye or skin contact occurs, rinse immediately with water. Operators should wash thoroughly with soap and water after handling Cattlyst 50G.
Keep container closed between uses.
Store below 25°C (77°F), excursions permitted to 37°C (99°F).
Restricted Drug (California) - Use Only as Directed. Not for human use.
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INGREDIENTS AND APPEARANCE
CATTLYST
laidlomycin propionate potassium granuleProduct Information Product Type OTC TYPE A MEDICATED ARTICLE ANIMAL DRUG Item Code (Source) NDC:54771-2000 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LAIDLOMYCIN PROPIONATE POTASSIUM (UNII: 05TAA9I0Z8) (LAIDLOMYCIN - UNII:MI3S6ZF5QE) LAIDLOMYCIN 50 g in 0.45 kg Product Characteristics Color white (white to off white) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54771-2000-1 22.68 kg in 1 BAG Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NADA NADA141025 01/01/2009 Labeler - Zoetis Inc. (828851555)