Label: 70 ALCOHOL HAND SANITIZER- alcohol liquid

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

Drug Label Information

Updated February 17, 2026

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  • DOSAGE & ADMINISTRATION

    Thoroughly cover your hands with product and allow to dry without wiping. Children under 6 years of age should be supervised when using this product. Not recommended for infants.

  • INDICATIONS & USAGE

    To decrease bacteria on the skin that could cause disease. Recommended for repeated use.

  • INACTIVE INGREDIENT

    purified water, methyl salicylate, FD&C Blue #1, FD&C Yellow #5

  • ACTIVE INGREDIENT

    70% Ethyl Alcohol

  • WARNINGS

    For external use only: hands. Flammable, Keep away from fire of flame.

  • ASK DOCTOR

    Irritation or redness develops. Condition persist for more than 72 hours.

  • KEEP OUT OF REACH OF CHILDREN

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

  • OTHER SAFETY INFORMATION

    Store below 105°F. May discolor some fabrics. Harmful to wood finishes and plastic

  • PURPOSE

    Antiseptic Alcoho

  • WHEN USING

    Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.

  • PRINCIPAL DISPLAY PANEL

    WinterGreen 70Wintergreen 70

  • INGREDIENTS AND APPEARANCE
    70 ALCOHOL HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74375-060
    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
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    WATER (UNII: 059QF0KO0R)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74375-060-01355 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/07/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00304/07/2025
    Labeler - Iron Lab SA de CV (951575800)
    Registrant - Iron Lab SA de CV (951575800)
    Establishment
    NameAddressID/FEIBusiness Operations
    Iron Lab SA de CV951575800manufacture(74375-060)
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