Label: KETO-C XL WIPES 60 COUNT- chlorhexidine gluconate, ketoconazole cloth
- NDC Code(s): 86069-115-60
- Packager: Stratford Care Usa, Inc.
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated November 21, 2022
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- ACTIVE INGREDIENT
- PURPOSE
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INDICATIONS & USAGE
Keto-C® XL Wipes contain an antiseptic (antibacterial and antifungal) solution for the topical management of skin conditions that are responsive to chlorhexidine and ketoconazole. Keto-C® XL Wipes can be used for the antiseptic cleansing of face folds, finger folds, as well as underarms and groin areas.
- INACTIVE INGREDIENT
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DOSAGE & ADMINISTRATION
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 Keto-C® Flush instead).
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PRECAUTIONS
Cautions: For animal use only. For topical use only. Avoid contact with eyes or mucous membranes. If undue skin irritation develops or increases, discontinue use and consult your veterinarian. In case of contact, flush eyes with water and seek medical attention if undue irritation persists. Keep out of the reach of children.
- STORAGE AND HANDLING
- SPL UNCLASSIFIED SECTION
- Packaging
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INGREDIENTS AND APPEARANCE
KETO-C XL WIPES 60 COUNT
chlorhexidine gluconate, ketoconazole clothProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:86069-115 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) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERIN (UNII: PDC6A3C0OX) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:86069-115-60 60 in 1 CONTAINER 1 0.15 mL in 1 PACKAGE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/01/2021 Labeler - Stratford Care Usa, Inc. (036650469)
