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. Do not allow the animal to lick the area(s) 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

wipe006

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: 3/2023
 
Holden2 LLC