HAND SANITIZER  - alcohol gel 
HOME DEPOT U.S.A. INC.

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.

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ACTIVE INGREDIENT:
ETHYL ALCOHOL 64% V/V

PURPOSE:

ANTISEPTIC

USES

for hand washing to decrease bacteria on the skin (safe for repeated use)

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.

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

Water, Polysorbate 20, Phenoxyethanol, Glycerin, Tromethamine, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Extract, Chamomilla Recutital (Matricaria) Flower Extract, Cucumis Sativus (Cucumber) Fruit Extract, Althaea Officinalis Root Extract, DL-Alpha Tocopheryl Acetate (Vitamin E) and Fragrance.

HDX

8 OZ HAND SANITIZER

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HAND SANITIZER 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42584-1000
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL64 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
POLYSORBATE 20 
PHENOXYETHANOL 
GLYCERIN 
TROMETHAMINE 
CARBOMER INTERPOLYMER TYPE A (55000 MPA.S) 
ALOE VERA LEAF 
CHAMOMILE 
CUCUMBER JUICE 
ALTHAEA OFFICINALIS ROOT 
.ALPHA.-TOCOPHEROL ACETATE, D- 
Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMultilevel Packaging
1NDC:42584-1000-8236 mL in 1 BOTTLE, PUMPNone
2NDC:42584-1000-21 BOTTLE ( BOTTLE) in 1 BLISTER PACKcontains a BOTTLE (42584-1000-1)
2NDC:42584-1000-153 mL in 1 BOTTLEThis package is contained within the BLISTER PACK (42584-1000-2)

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: 02/2012 HOME DEPOT U.S.A. INC.