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HAND SANITIZER by HOME DEPOT U.S.A. INC.

Dosage form: gel
Ingredients: ALCOHOL 62mL in 100mL
Labeler: HOME DEPOT U.S.A. INC.
NDC Code: 42584-1001

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

ACTIVE INGREDIENT
ETHYL ALCOHOL 62% V/V

PURPOSE:

ANTISEPTIC

USES

HAND SANITIZER TO HELP REDUCE BACTERIA ON SKIN THAT COULD CAUSE DISEASE

Warnings
For external use only

Flammable, keep away from fire or flame

Other information Do not store above 110F (43C).
Store in an area inaccessible to children.

When using this product
■ Avoid contact with eyes. If in eyes, flush with water.

■ Do not ingest.

■ Discontinue use and contact a doctor if irritation and redness develop and conditions persist for more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately. In case of transportaton or first aid emergency contact CHEMTEL 1-800-255-3924.

Directions

Place small amount in your palm and rub hands together until dry. Children under 6 years of age should be supervised when using this product.

Inactive ingredients

Aloe Vera Extract, Carbomer, Fragrance, Glycerin, Isopropyl Alcohol, Isopropyl Myristate, Propylene Glycol, Tocopheryl Acetate,
Vitamin E, Water.

HAND SANITIZER 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42584-1001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL62 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF 
CARBOMER 940 
GLYCERIN 
ISOPROPYL ALCOHOL 
ISOPROPYL MYRISTATE 
PROPYLENE GLYCOL 
.ALPHA.-TOCOPHEROL ACETATE, D- 
WATER 
Packaging
#Item CodePackage Description
1NDC:42584-1001-8236 mL in 1 BOTTLE, PUMP
2NDC:42584-1001-21 BOTTLE (BOTTLE) in 1 BLISTER PACK
2NDC:42584-1001-153 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E02/14/2012
Labeler - HOME DEPOT U.S.A. INC. (783266950)

Revised: 04/2013
 
HOME DEPOT U.S.A. INC.

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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