PURELL VF481 HAND SANITIZER (ALCOHOL) GEL [GOJO INDUSTRIES, INC.]

PURELL VF481 HAND SANITIZER (ALCOHOL) GEL [GOJO INDUSTRIES, INC.]
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NDC 21749-526-02, 21749-526-89, 21749-526-97
Set ID 085a209c-83a1-413c-ac70-3b415d6186cf
Category HUMAN OTC DRUG LABEL
Packager GOJO Industries, Inc.
Generic Name
Product Class
Product Number
Application Number PART333E
  • Active ingredient

    Ethyl alcohol 70% v/v

  • Purpose

    Antimicrobial

  • Use

    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 thoroughly cover your 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, Copper Gluconate, Diisopropyl Sebacate, PEG/PPG-20/6 Dimethicone, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Polyquaternium-37

  • PRINCIPAL DISPLAY PANEL

    Product Label

  • INGREDIENTS AND APPEARANCE
    PURELL VF481 HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-526
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.70 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Isopropyl Alcohol (UNII: ND2M416302)  
    Copper Gluconate (UNII: RV823G6G67)  
    Diisopropyl Sebacate (UNII: J8T3X564IH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21749-526-0259 mL in 1 BOTTLE; Type 0: Not a Combination Product05/26/2010
    2NDC:21749-526-97700 mL in 1 BOTTLE; Type 0: Not a Combination Product05/26/2010
    3NDC:21749-526-891200 mL in 1 BOTTLE; Type 0: Not a Combination Product05/26/2010
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E05/26/2010
    Labeler - GOJO Industries, Inc. (004162038)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.036424534manufacture(21749-526)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.088312414manufacture(21749-526) , label(21749-526) , pack(21749-526)

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