Label: PURELL ADVANCED INSTANT HAND SANITIZER- alcohol liquid

  • NDC Code(s): 21749-807-17, 21749-807-22, 21749-807-23, 21749-807-30, view more
    21749-807-31, 21749-807-33, 21749-807-50, 21749-807-51, 21749-807-53, 21749-807-80, 21749-807-89, 21749-807-97
  • Packager: GOJO Industries, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 13, 2024

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  • Active ingredient

    Ethyl Alcohol 70%

  • Purpose

    Antimicrobial

  • Use

    Hand sanitizer to help reduce bacteria on the skin that could cause disease

  • 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 ifirritation 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 thoroughly cover your hands. 

    Rub hands together briskly until dry.

    Children under 6 years of age should be supervised when using this product.

  • Other information

    Store below 110 oF (43 oC)

    May discolor certain fabrics or surfaces

  • Inactive ingredients

    Water (Aqua), Isopropyl Alcohol, PEG-12 Dimethicone, Caprylyl Glycol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Fragrance (Parfum)

  • PRINCIPAL DISPLAY PANEL

    Product Label

  • INGREDIENTS AND APPEARANCE
    PURELL ADVANCED INSTANT HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-807
    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)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21749-807-3145 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/11/201101/31/2024
    2NDC:21749-807-22200 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/11/201112/13/2024
    3NDC:21749-807-23222 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/11/201112/13/2024
    4NDC:21749-807-17515 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/13/2022
    5NDC:21749-807-53535 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/11/2011
    6NDC:21749-807-51550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/11/2011
    7NDC:21749-807-331000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/11/2011
    8NDC:21749-807-891200 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/11/2011
    9NDC:21749-807-97700 mL in 1 PACKAGE; Type 0: Not a Combination Product04/11/2011
    10NDC:21749-807-30300 mL in 1 PACKAGE; Type 0: Not a Combination Product08/24/202012/13/2024
    11NDC:21749-807-50189271 mL in 1 PACKAGE; Type 0: Not a Combination Product08/24/2020
    12NDC:21749-807-80800 mL in 1 PACKAGE; Type 0: Not a Combination Product02/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/11/2011
    Labeler - GOJO Industries, Inc. (004162038)
    Registrant - GOJO Industries, Inc. (004162038)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.036424534manufacture(21749-807)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.088312414manufacture(21749-807) , label(21749-807) , pack(21749-807)
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