Label: PURELL ADVANCED HAND SANITIZER ULTRA NOURISHING FOAM- alcohol liquid

  • NDC Code(s): 21749-856-17, 21749-856-40
  • Packager: GOJO Industries, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 16, 2024

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  • Active ingredient

    Ethyl Alcohol 70% v/v

  • Purpose

    Antimicrobial

  • Uses

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

    • Recommended for repeated use

  • 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.

  • Directions

    • Place enough product in your palm to thoroughly cover your hands

    • Rub hands together briskly until dry

  • Inactive ingredients

    Water (Aqua), Isopropyl Alcohol, PEG-12 Dimethicone, Avena Sativa (Oat) Kernel Extract, Caprylyl glycol, Glycerin, Niaciniamide, PPG-12/SMDI copolymer, Potassium Sorbate

  • PRINCIPAL DISPLAY PANEL

    Product Label

  • INGREDIENTS AND APPEARANCE
    PURELL ADVANCED HAND SANITIZER ULTRA NOURISHING FOAM 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-856
    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)  
    PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)  
    OAT (UNII: Z6J799EAJK)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    PPG-12/SMDI COPOLYMER (UNII: 1BK9DDD24E)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21749-856-17515 mL in 1 BOTTLE; Type 0: Not a Combination Product12/04/2023
    2NDC:21749-856-401200 mL in 1 BOTTLE; Type 0: Not a Combination Product12/04/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)12/04/2023
    Labeler - GOJO Industries, Inc. (004162038)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.036424534manufacture(21749-856) , pack(21749-856) , label(21749-856)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.088312414manufacture(21749-856) , pack(21749-856) , label(21749-856)
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