Label: PURELL HEALTHCARE ADVANCED HAND SANITIZER GEL- alcohol gel

  • NDC Code(s): 21749-716-01, 21749-716-02, 21749-716-04, 21749-716-08, view more
    21749-716-12, 21749-716-20, 21749-716-89
  • 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 productdo 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 product on hands
    • Rub until dry
  • Inactive ingredients

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

  • PRINCIPAL DISPLAY PANEL

    Product Label

  • INGREDIENTS AND APPEARANCE
    PURELL HEALTHCARE ADVANCED HAND SANITIZER GEL 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-716
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21749-716-0129 mL in 1 BOTTLE; Type 0: Not a Combination Product10/15/201703/31/2022
    2NDC:21749-716-0259 mL in 1 BOTTLE; Type 0: Not a Combination Product10/15/201705/31/2022
    3NDC:21749-716-04118 mL in 1 BOTTLE; Type 0: Not a Combination Product10/15/201712/11/2024
    4NDC:21749-716-08236 mL in 1 BOTTLE; Type 0: Not a Combination Product10/15/201712/11/2024
    5NDC:21749-716-12354 mL in 1 BOTTLE; Type 0: Not a Combination Product10/15/201712/11/2024
    6NDC:21749-716-891200 mL in 1 BOTTLE; Type 0: Not a Combination Product10/15/2017
    7NDC:21749-716-202000 mL in 1 PACKAGE; Type 0: Not a Combination Product10/15/201712/11/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)10/15/2017
    Labeler - GOJO Industries, Inc. (004162038)
    Registrant - GOJO Industries, Inc. (004162038)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.036424534manufacture(21749-716)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.088312414manufacture(21749-716) , label(21749-716) , pack(21749-716)
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