Label: PURELL ADVANCED MOISTURIZING 2IN1- alcohol gel

  • NDC Code(s): 21749-751-04, 21749-751-12
  • Packager: GOJO Industries, Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 11, 2024

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  • Active ingredient

    Ethyl alcohol 70% v/v

  • Purpose

    Antimicrobial

  • Uses

    • Hand sanitizer to help reduce bacteria on the skin
  • Warnings

    Flammable. Keep away from fire or flame.

    For external use only

    When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

    Stop use and ask a doctor if irritation or rash appears and lasts

    Keep Out of Reach of Children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Place enough product in your palm to cover hands
    • Rub hands together briskly until dry
    • Children under 6 years of age should be supervised when using this product
  • Inactive ingredients

    Water (Aqua), Isopropyl Alcohol, Glycerin, Caprylyl Glycol, Isopropyl Myristate, Linum Usitatissimum (Linseed) Seed Extract, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum)

  • Product Label

    Product Label

  • INGREDIENTS AND APPEARANCE
    PURELL ADVANCED MOISTURIZING 2IN1 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-751
    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
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    FLAX SEED (UNII: 4110YT348C)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21749-751-04118 mL in 1 BOTTLE; Type 0: Not a Combination Product01/25/2021
    2NDC:21749-751-12354 mL in 1 BOTTLE; Type 0: Not a Combination Product01/25/202112/11/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/25/2021
    Labeler - GOJO Industries, Inc. (004162038)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.036424534manufacture(21749-751) , pack(21749-751) , label(21749-751)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.088312414manufacture(21749-751) , label(21749-751) , pack(21749-751)
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