Label: PURELL ADVANCED SKIN NOURISHING INSTANT HAND SANITIZER- alcohol liquid

  • NDC Code(s): 21749-801-31, 21749-801-33, 21749-801-53, 21749-801-89, view more
    21749-801-97
  • Packager: GOJO Industries, Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 12, 2024

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  • Active Ingredient

    Ethyl Alcohol 70% v/v

  • Purpose

    Antimicrobial

  • Use

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

  • 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
  • WARNINGS

    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 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.

  • Inactive ingredients

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

  • PRINCIPAL DISPLAY PANEL

    Product Label

  • INGREDIENTS AND APPEARANCE
    PURELL ADVANCED SKIN NOURISHING INSTANT HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-801
    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)  
    PEG-12 DIMETHICONE (UNII: ZEL54N6W95)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21749-801-3145 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/201112/31/2023
    2NDC:21749-801-331000 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/201106/30/2022
    3NDC:21749-801-53535 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/201105/31/2024
    4NDC:21749-801-97700 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/201102/28/2023
    5NDC:21749-801-891200 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/2011
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)08/01/2011
    Labeler - GOJO Industries, Inc. (004162038)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.036424534manufacture(21749-801)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.088312414manufacture(21749-801) , label(21749-801) , pack(21749-801)
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