Label: FRESH HAND FOAMING HAND SANITIZER ALCOHOL FOAM- ethyl alcohol solution

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated September 21, 2023

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  • Active ingredient

    Ethyl Alcohol 70 %

    Purpose

    Antibacterial

  • PURPOSE

    ANTIBACTERIAL

  • Uses

    • Hand sanitizer to help reduce bacteria on the skin.
  • WARNINGS

    Flammable. Keep away from fire or flame.

    For external use only.

    When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

    Stop use and ask a doctor if irritation or rash appears and lasts.

    When using this product

    • avoid contact with eyes. In case of eye contact, flush with water

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • DIRECTIONS

    • Place enough product on your palm to thoroughly cover your hands
    • Rub hands together briskly until dry

  • Inactive ingredients

    Water, Isopropyl Alcohol, Propylene Glycol, PEG-12 Dimethicone Crosspolymer, BIS-PEG-12 Dimethicone.

  • PRINCIPAL DISPLAY PANEL

    01b LBL_Fresh Hand_Foaming Hand Sanitizer_Alcohol Foam

  • INGREDIENTS AND APPEARANCE
    FRESH HAND FOAMING HAND SANITIZER ALCOHOL FOAM 
    ethyl alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70415-203
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)  
    BIS-PEG-12 DIMETHICONE (70 MPA.S) (UNII: 2JDK5W22H4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70415-203-111000 mL in 1 BOTTLE; Type 0: Not a Combination Product08/04/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00308/04/2020
    Labeler - CWGC LA Inc. (034967904)
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