HEXACHLOR-K WIPES- chlorhexidine gluconate and ketoconazole cloth

HexaChlor-K Wipes by

Drug Labeling and Warnings

HexaChlor-K Wipes by is a Animal medication manufactured, distributed, or labeled by GlenHaven LLC, Dechra Veterinary Products. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

VETERINARY INDICATIONS

HexoChlor-K Wipes promote healthy skin for animals with conditions responsive to ketoconozole and/or chlorhexidine.

DESCRIPTION

ACTIVE INGREDIENTS: 2% Chlorhexidine Gluconote, USP; 1% Ketoconozole, USP.

SPL UNCLASSIFIED SECTION

ALSO CONTAINS: Purified Water, Propylene Glycol, PEG 5 Cocomide, Polyethylene Glycol 600, Benzyl Alcohol, Acetic Acid, OP-10, Fragrance.

DOSAGE & ADMINISTRATION

DIRECTIONS: Apply to affected area as directed by your veterinarian.

PRECAUTIONS

CAUTION: If skin irritation develops or increases, stop use and call your veterinarian. Keep out of the reach of children and pets.

SAFE HANDLING WARNING

HUMAN WARNING: Wash hands after use. Rare but serious allergic reactions have been reported with exposure to chlorhexidine gluconate.

STORAGE AND HANDLING

STORAGE: Store at room temperature.

SPL UNCLASSIFIED SECTION

Available through licensed veterinarians.

SPL UNCLASSIFIED SECTION

Manufactured for:
GlenHaven
18101 SE 6th Way
Vancouver, WA
98683

39648 REV04/20

Antimicrobial,
antifungal

Acetic acid,
chlorhexidine,
ketoconazole

PRINCIPAL DISPLAY PANEL - 50 Wipe Container Label

GlenHaven®
Therapeutics

Medically Formulated

HexaChlor-K Wipes

Formerly F3/W
For Dog and Cat Use Only
Net Contents: 50 Wipes

INGREDIENTS AND APPEARANCE

HEXACHLOR-K WIPES 
chlorhexidine gluconate and ketoconazole cloth

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 70782-183
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L)	CHLORHEXIDINE GLUCONATE	20 mg
KETOCONAZOLE (UNII: R9400W927I) (KETOCONAZOLE - UNII:R9400W927I)	KETOCONAZOLE	10 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70782-183-50	50 in 1 CONTAINER

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
UNAPPROVED DRUG OTHER		01/21/2021

Labeler - GlenHaven LLC (002542300)