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

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PURELL PROFESSIONAL ADVANCED HAND SANITIZER GEL (ALCOHOL) GEL [GOJO INDUSTRIES, INC.]
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NDC 21749-715-08, 21749-715-10, 21749-715-12, 21749-715-20, 21749-715-89
Set ID 5a6cf5f6-82d0-4aae-a722-53ce3a83d264
Category HUMAN OTC DRUG LABEL
Packager GOJO Industries, Inc.
Generic Name
Product Class
Product Number
Application Number PART333E
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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 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 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 PROFESSIONAL ADVANCED HAND SANITIZER GEL 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-715
    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:21749-715-08236 mL in 1 BOTTLE; Type 0: Not a Combination Product10/15/2017
    2NDC:21749-715-12354 mL in 1 BOTTLE; Type 0: Not a Combination Product10/15/2017
    3NDC:21749-715-101000 mL in 1 BOTTLE; Type 0: Not a Combination Product10/15/2017
    4NDC:21749-715-891200 mL in 1 BOTTLE; Type 0: Not a Combination Product10/15/2017
    5NDC:21749-715-202000 mL in 1 PACKAGE; Type 0: Not a Combination Product10/15/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E10/15/2017
    Labeler - GOJO Industries, Inc. (004162038)
    Registrant - GOJO Industries, Inc. (004162038)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.036424534MANUFACTURE(21749-715)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.088312414MANUFACTURE(21749-715) , label(21749-715) , pack(21749-715)
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