Label: TOXIBAN- activated charcoal granule
- NDC Code(s): 11789-042-20, 11789-042-30
- Packager: LLOYD, Inc. of Iowa
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated July 11, 2023
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- VETERINARY INDICATIONS
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DOSAGE & ADMINISTRATION
DOSAGE AND ADMINISTRATION:
Large Animals – The recommended dosage is 0.75 to 2.0 grams per kg (0.35 to 0.9 grams per lb) body weight. One pound (454 grams) can normally treat an animal weighing 225 to 600 kg (500 to 1,300 lb). Prepare a suspension by mixing one part of ToxiBan Granules with 5 to 7 parts (volume/volume measures) of cold water. Shake or stir vigorously for 10 seconds. Under the direction of a veterinarian, deliver into stomach or rumen, preferably through a stomach tube and funnel or stomach pump. Rinse container and equipment with cold water and administer to the animal before removing the stomach tube.
Small Animals – The recommended dosage is 2 to 4 grams per kg (1 to 2 grams per lb) body weight. Prepare a suspension by mixing one part of ToxiBan Granules with 5 to 7 parts (volume/volume measures) of cold water. Shake or stir vigorously for 10 seconds. Give orally by encouraging the animal to drink the calculated dose. Consult a veterinarian should administration by stomach tube be needed. ToxiBan Suspension or ToxiBan Suspension with Sorbitol may be more convenient for use in small animals.
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- STORAGE AND HANDLING
- PRECAUTIONS
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PRINCIPAL DISPLAY PANEL - 5 kg Pail Label
NDC 11789-042-20
ToxiBan® Granules
Water Miscible Charcoal-Sorbitol-KaolinINDICATION:
For use as a decontamination agent via
adsorption of organic chemical toxicants in
domestic animals.In all cases of suspected poisonings,
consult your veterinarian for complete
diagnosis and specific treatment.LLOYD®
Net Weight: 5 kg (11.02 lb)
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INGREDIENTS AND APPEARANCE
TOXIBAN
activated charcoal granuleProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:11789-042 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL 240 [arb'U] in 1 g Inactive Ingredients Ingredient Name Strength KAOLIN (UNII: 24H4NWX5CO) SORBITOL (UNII: 506T60A25R) Product Characteristics Color BLACK (BLACK GRANULATED POWDER) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11789-042-30 453.6 g in 1 BOTTLE 2 NDC:11789-042-20 5000 g in 1 PAIL Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED DRUG OTHER 07/07/2023 Labeler - LLOYD, Inc. of Iowa (962286535) Registrant - LLOYD, Inc. of Iowa (007281942) Establishment Name Address ID/FEI Business Operations LLOYD, Inc. of Iowa 962286535 LABEL, API MANUFACTURE, PACK, MANUFACTURE Establishment Name Address ID/FEI Business Operations LLOYD, Inc. of Iowa 007281942 ANALYSIS