Label: PHARMASEB WIPES- chlorhexidine gluconate, ketoconazole cloth
- NDC Code(s): 68898-119-50
- Packager: Animal Pharmaceuticals
- 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 November 18, 2022
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients (per wipe)
- Purpose
- Inactive Ingredients
- Precautions
- Cautions
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Directions for use
Thoroughly wipe affected area with a pad 1 to 3 times per day, or as directed by your veterinarian. Do not allow the animal to lick the treated areas until dry to prevent ingestion. Wipes should be used for one application only; do not reuse. Avoid use on open wounds, cuts or raw areas (use Pharmaseb Flush instead).
- Other information
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SPL UNCLASSIFIED SECTION
An antifungal and antimicrobial wipe
Formulated with Ketoconazole and Chlorhexidine
Cucumber Melon
Formulated for Dogs, Cats & Horses
A water-based, antifungal and antibacterial wipe, synergistically formulated with Ketoconazole and Chlorhexidine. Provides generalized topical therapy of dermatitis in dogs, cats and horses.
MANUFACTURED FOR
Animal Pharmaceuticals
www.anmpharm.comMADE IN THE USA
- Packaging
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INGREDIENTS AND APPEARANCE
PHARMASEB WIPES
chlorhexidine gluconate, ketoconazole clothProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:68898-119 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE 2 g in 100 mL KETOCONAZOLE (UNII: R9400W927I) (KETOCONAZOLE - UNII:R9400W927I) KETOCONAZOLE 1 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) NONOXYNOL-9 (UNII: 48Q180SH9T) LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT) POLYSORBATE 20 (UNII: 7T1F30V5YH) GLYCERIN (UNII: PDC6A3C0OX) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68898-119-50 50 in 1 JAR 1 1 mL in 1 PACKAGE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/05/2021 Labeler - Animal Pharmaceuticals (166472444) Registrant - Stratford Care Usa, Inc. (036650469)