HAND SANITIZER (ETHYL ALCOHOL) GEL [HOME DEPOT U.S.A. INC.]

HAND SANITIZER (ETHYL ALCOHOL) GEL [HOME DEPOT U.S.A. INC.]
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NDC 42584-1001-1, 42584-1001-2, 42584-1001-8
Set ID cbd19a50-83ce-4fc7-b2ce-881d5ce06069
Category HUMAN OTC DRUG LABEL
Packager HOME DEPOT U.S.A. INC.
Generic Name
Product Class
Product Number
Application Number PART333E
  • ACTIVE INGREDIENT

    ACTIVE INGREDIENT
    ETHYL ALCOHOL 62% V/V

  • PURPOSE

    PURPOSE:

    ANTISEPTIC

  • INDICATIONS & USAGE

    USES

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

  • WARNINGS

    Warnings
    For external use only

    Flammable, keep away from fire or flame

  • OTHER SAFETY INFORMATION

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

  • WHEN USING

    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

    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.

  • DOSAGE & ADMINISTRATION

    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 INGREDIENT

    Inactive ingredients

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

  • PRINCIPAL DISPLAY PANEL

    HDX_Sanitizer_ART_2oz_Blister-FR 2012-05-03

    HDX_Sanitizer_ART_2oz_LBL_BK 2012-05-03

    HDX_Sanitizer_ART_2oz_LBL_FR 2012-05-03

    HDX_Sanitizer_ART_8oz_LBL_2013-04-08

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42584-1001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42584-1001-8236 mL in 1 BOTTLE, PUMP
    2NDC:42584-1001-21 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)

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