Label: PURELL ADVANCED REFRESHING - alcohol gel 

  • NDC Code(s): 21749-704-01, 21749-704-02, 21749-704-04, 21749-704-08, view more
    21749-704-12
  • Packager: GOJO Industries, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 10/12

If you are a consumer or patient please visit this version.

  • Active ingredient

    Ethyl alcohol 70% v/v

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  • Purpose

    Antimicrobial

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  • Uses

    • Hand sanitizer to help reduce bacteria on the skin
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  • Warnings

    Flammable. Keep away from fire or flame.

    For external use only

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  • When using this product

    do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

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  • 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.

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  • Directions

    • Put enough product in your palm to cover hands and rub hands together briskly until dry
    • Children under 6 years of age should be supervised when using PURELL
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  • Other information

    • Store below 110°F (43°C)
    • May discolor certain fabrics or surfaces
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  • Inactive ingredients

    Water (Aqua), Isopropyl Alcohol, Caprylyl Glycol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum)

    Distributed by:
    GOJO Industries, Inc.
    Akron, OH 44309
    Questions?
    Tel: 1-888-4-PURELL
    www.PURELL.com
    ©2011.
    GOJO Industries, Inc.
    All rights reserved.
    Made in U.S.A.

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  • Package/Label Principal Display Panel

    New!
    More Effective Formula

    Purell 
    ADAVANCED
    Hand Sanitizer

    KILLS THE MOST GERMS

    Refreshing Gel

    Kills More Than 99.99% of Germs
    Leaves Hands Feeling Soft

    2 FL OZ (59 mL)


    Bottle Label

    Bottle Label

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  • INGREDIENTS AND APPEARANCE
    PURELL ADVANCED REFRESHING 
    alcohol gel
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:21749-704
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (ALCOHOL) ALCOHOL 0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    ISOPROPYL ALCOHOL  
    CAPRYLYL GLYCOL  
    GLYCERIN  
    ISOPROPYL MYRISTATE  
    .ALPHA.-TOCOPHEROL ACETATE, D-  
    AMINOMETHYLPROPANOL  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:21749-704-01 29 mL in 1 BOTTLE
    2 NDC:21749-704-02 59 mL in 1 BOTTLE
    3 NDC:21749-704-08 236 mL in 1 BOTTLE
    4 NDC:21749-704-12 354 mL in 1 BOTTLE
    5 NDC:21749-704-04 118 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 03/15/2012
    Labeler - GOJO Industries, Inc. (004162038)
    Establishment
    Name Address ID/FEI Business Operations
    GOJO Industries, Inc. 036424534 MANUFACTURE(21749-704)
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