Label: AMERICAN RED CROSS ADVANCED SANITIZER ETHYL ALCOHOL- ethyl alcohol aerosol, spray

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

Drug Label Information

Updated December 25, 2024

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  • Active ingredient

    Ethyl Alcohol 70%

  • Purpose

    Antiseptic

  • Uses

    • effective in reducing bacteria on the skin.
    • recommended for repeated use.
  • Warnings

    For external use only.

    • Flammable: keep away from heat, spark, electrical, fire, and flame. Contents under pressure.
    • Do not puncture or incinerate. Do not store at temperatures above 122F (50C).
    • Use only in well ventilated area; fumes may be harmful.

    When using this product

    • Keep out of eyes. In case of eye contact, flush eyes with water.
    • Avoid contact with broken skin or open wounds.

    Stop use and seek medical advisement

    If irritation and redness develop.

    Keep out of reach of children

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

  • Directions

    • Spray directly on hands.
    • Rub hands together for 15 seconds, paying attention to fingernails, cuticles, and the space between fingers.
    • Allow to dry without wiping.
  • Inactive ingredients

    Water(Auqa)

    Propane/Isobutane

    Sodium Benzoate

    Aminomethyl propanol

  • Label

    label

  • INGREDIENTS AND APPEARANCE
    AMERICAN RED CROSS ADVANCED SANITIZER ETHYL ALCOHOL 
    ethyl alcohol aerosol, spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51628-4441
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPANE (UNII: T75W9911L6)  
    ISOBUTANE (UNII: BXR49TP611)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51628-4441-185 g in 1 BOTTLE; Type 0: Not a Combination Product12/26/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00312/26/2024
    Labeler - MY IMPORTS USA LLC (195767988)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang Guoyao Jingyue Aerosol Co., Ltd.554529812manufacture(51628-4441)
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