Label: CLEAN CHOICE ALCOHOL SANITIZER- ethyl alcohol liquid

  • NDC Code(s): 11084-704-12, 11084-704-27
  • Packager: Deb USA, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by 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 August 28, 2017

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

  • Active ingredient

    ETHYL ALCOHOL 70% w/w

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  • Purpose

    Antibacterial

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  • Uses

    for hand sanitizing to reduce bacteria on the skin

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  • Warnings

    For external use only

    Flammable.

    Keep away from fire or flame.

    When using this product

    avoid contact with eyes.  In case of eye contact, flush with water.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

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  • Directions

    apply foaming sanitizer to cover hands

    rub into skin

    no rinsing required

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  • Inactive ingredients

    AQUA (WATER), BEHENTRIMONIUM CHLORIDE, BIS-PEG-12 DIMETHICONE, COCO-GLUCOSIDE, DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE, GLYCERYL OLEATE, PEG-200 HYDROGENATED GLYCERYL PALMATE, PEG-7 GLYCERYL COCOATE.

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  • PRINCIPAL DISPLAY PANEL

    0617388-DCN9254 Instant Sanitizer-V9.jpg

    Clean Choice

    NDC 11084-704-12

    Foaming Alcohol Hand Sanitizer

    UL ECOLOGO

    PRODUCTS CERTIFIED FOR REDUCED ENVIRONMENTAL IMPACT.  VIEW SPECIFIC ATTRIBUTES EVALUATED: UL.COM/EL

    UL 2783

    1 L (33.8 fl oz)

    Stock # 0617388

    DCN9254/0517

    L-1417 R0

    Distributed Exclusively by Fastenal

    Distributed by Fastenal Company and its Subsidiaries

    Winona, MN 55987

    (C)2017 fastenal.com

    Made in Canada

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  • INGREDIENTS AND APPEARANCE
    CLEAN CHOICE ALCOHOL SANITIZER 
    ethyl alcohol liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:11084-704
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 L  in 100 L
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)  
    BIS-PEG-12 DIMETHICONE (500 MPA.S) (UNII: 2CNS542YRT)  
    COCO GLUCOSIDE (UNII: ICS790225B)  
    DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)  
    GLYCERYL OLEATE (UNII: 4PC054V79P)  
    PEG-200 HYDROGENATED GLYCERYL PALMATE (UNII: W161T051Y1)  
    PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:11084-704-27 1 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/15/2013
    2 NDC:11084-704-12 1 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/28/2017
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 09/15/2013
    Labeler - Deb USA, Inc. (607378015)
    Establishment
    Name Address ID/FEI Business Operations
    Deb Worldwide Healthcare Inc. 205662831 manufacture(11084-704)
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