Label: STYPTIC POWDER- ferric subsulfate powder
- NDC Code(s): 47082-400-15
- Packager: Westwood Laboratories Inc.
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated October 6, 2021
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- ACTIVE INGREDIENTS
- INSTRUCTIONS FOR USE
- CAUTION
- DIRECTIONS
- OTHER INGREDIENTS
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DESCRIPTION
Stop bleeding will quickly stop blood due to clipping nails or wings, or for minor, superficialcuts to the skin such as nicks from shaving. It is not recommended for use on deep cuts that require stitches or on severe wounds or in body cavities.
You can apply Stop Bleeding powder directly to the bleeding area by pressing the toe nail directly in powder. You can also apply Stop Bleeding powder with a pre-moistened applicator (like a swab) dipped in Stop Bleeding powder. If using an applicator, use moderate pressure and hold on the area until bleeding stops. If you cannot get bleeding to stop using moderate pressure for 10-15 seconds, consult a veterinarian.
Dist. by (c)2016 Cardinal Laboratories, Inc.,
aka Cardinal Pet Care, Azusa, California 91702 USA
Devoted to Pets, People & The Planet
www.cardinalpet.com
Dogswell Remedy & Recovery
- PROFESSIONAL GROOMER'S STYPTIC POWDER For Dogs, Cats and Birds Stops Bleeding
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INGREDIENTS AND APPEARANCE
STYPTIC POWDER
ferric subsulfate powderProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:47082-400 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FERRIC SUBSULFATE (UNII: 3QJ8WS6V8H) (FERRIC CATION - UNII:91O4LML611) FERRIC CATION 35 g in 100 g Inactive Ingredients Ingredient Name Strength BENTONITE (UNII: A3N5ZCN45C) POTASSIUM SULFATE (UNII: 1K573LC5TV) DIATOMACEOUS EARTH (UNII: 2RF6EJ0M85) AMMONIUM CHLORIDE (UNII: 01Q9PC255D) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47082-400-15 42.5 g in 1 JAR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/01/1970 Labeler - Westwood Laboratories Inc. (832280635) Registrant - Westwood Laboratories Inc. (832280635) Establishment Name Address ID/FEI Business Operations Westwood Laboratories Inc. 832280635 manufacture, relabel, repack, api manufacture