Label: AMERICAN RED CROSS 70% ETHYL ALCOHOL HAND SANITIZER- ethyl alcohol gel

  • NDC Code(s): 75742-032-01
  • Packager: Zhejiang Guoyao Jingyue Aerosol Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 21, 2024

If you are a consumer or patient please visit this version.

  • Active ingredients

    Ethyl Alcohol 70% v/v

  • Purpose

    Antiseptic

  • Warnings

    For external use only.

    Flammable. Keep away from heat sparks, electrical, fire or flame.

    Do not apply around eyes.Do not use in ears & mouth.

    When using this product

    When using this product, avoid contact with eyes. In case of eye contact remove any contact lenses, and flush eyes with cold water. call a poison center or doctor/ physician.

    Keep out of reach of children

    Keep out of reach of children. Children must be supervised in use of this product.

    Stop use use and Seek

    Stop use use and Seek Medical sdvisement if irritation and Redness develop.

    If swallowed, do not induce vomiting. Seek immediate medical attention.

  • Uses

    Hand sanitizer to help decrease bacteria on the skin.

    When water, soap & towel are not available.

    Recommended for repeated use.

  • Directions

    • Pump as needed into your palms and thoroughly spread on both hands.
    • Rub into skin until dry.
  • Inactive Ingredients

    Water

    Glycerin

    Carbomer

    Propylene Glycol

    Aminomethyl Propanol

    Fragrance

    Aloe(Aloe barbadensis)Leaf Juice

    Tocopheryl Acetate

  • Hand Sanitizer 70% Ethyl Alcohol

    Enriched with Moisturizing

    Aloe Vera & Vitamin E

    8 FL OZ(236ml)

  • Other information

    • Store at 20ºC(68-77ºF)
    • May discolor fabrics
    • Questions/ Comment? Call toll-free:1-877-879-6999
  • Label

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  • INGREDIENTS AND APPEARANCE
    AMERICAN RED CROSS 70% ETHYL ALCOHOL HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75742-032
    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
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    WATER (UNII: 059QF0KO0R)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75742-032-01236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/21/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00303/21/2024
    Labeler - Zhejiang Guoyao Jingyue Aerosol Co., Ltd (554529812)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang Guoyao Jingyue Aerosol Co., Ltd.554529812manufacture(75742-032)