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HAND SANITIZER (HOME DEPOT U.S.A. INC.)

Available Formats

Dosage Form Package Information Links
GEL 1 BOTTLE in 1 BLISTER PACK (42584-1001-2) > 53 mL in 1 BOTTLE (42584-1001-1) Label Information
GEL 236 mL in 1 BOTTLE, PUMP (42584-1001-8) Label Information

Complete HAND SANITIZER Information

  • 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
    â–  Avoid contact with eyes. If in eyes, flush with water.

    â–  Do not ingest.

    â–  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.


  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:42584-1001
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mL  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    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 Code Package Description Marketing Start Date Marketing End Date
    1 NDC:42584-1001-8 236 mL in 1 BOTTLE, PUMP
    2 NDC:42584-1001-2 1 in 1 BLISTER PACK
    2 NDC:42584-1001-1 53 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 02/14/2012
    Labeler - HOME DEPOT U.S.A. INC. (783266950)