Label: ANTISEPSIS BOLUS- urea tablet
- NDC Code(s): 58005-762-02
- Packager: Sparhawk Laboratories, Inc.
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated April 28, 2014
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- INDICATIONS & USAGE
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PRECAUTION
Do not administer orally.
Strict cleanliness must be observed to prevent introduction of further infections. Thoroughly cleanse hands and arms of operator and external genital parts of the animal with soap and water before inserting boluses or flush.
Do not use in deep or puncture wounds or for serious burns.
- DOSAGE AND ADMINISTRATION
- COMPOSITION
- STORAGE AND HANDLING
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ANTISEPSIS BOLUS
urea tabletProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:58005-762 Route of Administration INTRAUTERINE, TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength UREA (UNII: 8W8T17847W) (UREA - UNII:8W8T17847W) UREA 13 g Product Characteristics Color pink (Pink) Score 2 pieces Shape OVAL (Oblong) Size 6mm Flavor Imprint Code ; Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58005-762-02 50 in 1 JAR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/01/1996 Labeler - Sparhawk Laboratories, Inc. (147979082)