PURELL ADVANCED SKIN NOURISHING INSTANT HAND SANITIZER (ALCOHOL) LIQUID [GOJO INDUSTRIES, INC.]

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PURELL ADVANCED SKIN NOURISHING INSTANT HAND SANITIZER (ALCOHOL) LIQUID [GOJO INDUSTRIES, INC.]
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NDC 21749-801-31, 21749-801-33, 21749-801-53, 21749-801-89, 21749-801-97
Set ID dfa86bfa-0f6a-4a9a-b968-3c15d4a2b2f4
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 that cause disease
    • Recommended for repeated use
  • 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
    • Run hands together briskly until dry
    • Children under 6 years of age should be supervised when using this product.
  • Inactive ingredients

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

  • Other information

    • Store below 110°F (43°C)
    • May discolor certain fabrics or surfaces
  • Package/Label Principal Display Panel

    NDC 21749-801-89

    PURELL
    ADVANCED SKIN NOURISHING
    INSTANT HAND SANITIZER FOAM

    Distributed by:
    GOJO Industries, Inc.
    Akron, OH 44309
    800-321-9647 • 330-255-6000
    www.GOJO.com
    ©2011. GOJO Industries, Inc. All rights reserved.
    Made in U.S.A.

    1200 mL (40.5 US/EU FL OZ)

    Bottle 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 (300 CST) (UNII: ZEL54N6W95)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21749-801-3145 mL in 1 BOTTLE
    2NDC:21749-801-53535 mL in 1 BOTTLE
    3NDC:21749-801-97700 mL in 1 BOTTLE
    4NDC:21749-801-331000 mL in 1 BOTTLE
    5NDC:21749-801-891200 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E12/21/2011
    Labeler - GOJO Industries, Inc. (004162038)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.036424534MANUFACTURE(21749-801)
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