Label: ANTISEPTIC HAND SANITIZER- ethyl alcohol gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated December 13, 2022

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  • Drug Facts

  • Active Ingredient

    Ethyl Alcohol 62%

  • Purpose

    Antiseptic

  • 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.

  • Use

    To help clean hands

  • Warnings

    Flammable, keep away from fire or flame. For external use only.

    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.

  • Directions

    Spread on both hands, rub in, let dry.

  • Inactive Ingredients

    Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate, Triethanolamine, Water.

  • Questions?

    Call 1-855-755-5346

  • SPL UNCLASSIFIED SECTION

    Made in China for Innovation Line Culver City, CA 90230

    Citrus Scent

  • Packaging

    Antiseptic sanitizer 15 ml

  • INGREDIENTS AND APPEARANCE
    ANTISEPTIC HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76138-113(NDC:70412-110)
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76138-113-161 in 1 BAG01/02/2016
    115 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/02/2016
    Labeler - Innovation Specialties Inc (030837314)
    Establishment
    NameAddressID/FEIBusiness Operations
    Innovation Specialties Inc030837314relabel(76138-113) , repack(76138-113)
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