Label: ANTIBACTERIAL HAND SANITIZER- ethyl alcohol gel

  • NDC Code(s): 70412-114-73
  • Packager: Zhejiang Ayan Biotech Co.,Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 6, 2023

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  • Drug Facts

  • Active Ingredients

    Ethyl Alcohol 62%

    Purpose

    Antiseptic

  • Uses:

    Hand sanitizer to help decrease bacteria on the skin. When water, soap & towel are not available.

    Recommended for repeated use.

  • Warnings:

    For external use only.

    Flammable. Keep away from fire or flame.

    Do not apply around eyes,

    Do not use

    in ears & mouth.

    When using this product,

    avoid contact with eyes. In case of contact flush eyes with water.

    Stop use and ask a doctor

    if redness or irritation develop and persist for more than 72 hours.

    Keep out of reach of children.

    Children must be supervised in use of this product.

  • Directions:

    Squirt as needed into your palms and thoroughly spread on both hands. Rub into skin until dry

  • Other Information:

    Store at 20°C (68° to 77°F). May discolor fabrics

  • Inactive Ingredients:

    water, triethanolamine, glycerin, propylene glycol, tocopheryl acetate, carbomer, fragrance.

  • Package Labeling:

    label

  • INGREDIENTS AND APPEARANCE
    ANTIBACTERIAL HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70412-114
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL620 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70412-114-731 in 1 BOX02/04/2016
    1473 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)02/04/2016
    Labeler - Zhejiang Ayan Biotech Co.,Ltd. (544377996)
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