KETOWELL XL WIPES- chlorhexidine gluconate, ketoconazole cloth 
Holden2 LLC

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.

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KetoWELL® XL Wipes

Active Ingredients:

Chlorhexidine Gluconate 2% and Ketoconazole 1%.

KetoWELL XL Wipes can be used for the cleansing of facial folds, finger folds, as well as underarm and groin areas.

Ingredients:

Water, Propylene Glycol, Nonoxynol-9, Lactic Acid, Polysorbate 20, Aloe Barbadensis (Aloe) Leaf Juice, Glycerin, Fragrance, Methylisothiazolinone.

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.

Precautions:

Avoid contact with eyes or mucous membranes. If eye contact occurs, rinse thoroughly with water and consult a veterinarian.

Cautions:

If undue skin irritation develops or increases, discontinue use and consult a veterinarian.

Storage:

Store at room temperature. Protect from freezing.

Formulated for Dogs & Cats

MFG IN USA

Manufactured for:
VetWELL®
Odessa, FL 33556
www.vetwell.com

Packaging

Holden2-006

KETOWELL XL WIPES 
chlorhexidine gluconate, ketoconazole cloth
Product Information
Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:86090-006
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE2 g  in 100 mL
KETOCONAZOLE (UNII: R9400W927I) (KETOCONAZOLE - UNII:R9400W927I) KETOCONAZOLE1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:86090-006-6060 in 1 CONTAINER
10.15 mL in 1 PACKAGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/04/2021
Labeler - Holden2 LLC (060164988)

Revised: 2/2023
 
Holden2 LLC