Label: CLEAN CHOICE FOODSERVICE ANTIBACTERIAL- benzalkonium chloride liquid

  • 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 09/13

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

  • Active ingredient

    Benzalkonium Chloride, 1.30%

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  • Purpose

    Antibacterial

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  • Uses

    For hand washing to reduce bacteria on the skin

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  • Warnings

    For external use only

    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 to dry hands

    Add water

    Lather hands for 30 seconds

    Rinse and dry hands thoroughly

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  • Inactive ingredients

    Water, Cocamidopropyl Betaine, Undeceth-7, Cocamidopropylamine Oxide, Lauramine Oxide, Tetrasodium EDTA, Citric Acid, Magnesium Nitrate, Methylchloroisothiazolinone, Magnesium Chloride, Methylisothiazolinone

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  • PRINCIPAL DISPLAY PANEL

    Clean Choice Foodservice Antibacterial Foam Soap

    1 L

    33.8 fl. oz.

    Part #0617377

    Distributed by Fastenal Co.

    Winona, MN  55987

    2013 fastenal.com

    Made in U.S.A.

    0617377

    Foodservice AntiBac Soap

    Rev. 08-13-11

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  • INGREDIENTS AND APPEARANCE
    CLEAN CHOICE FOODSERVICE ANTIBACTERIAL 
    benzalkonium chloride liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:11084-255
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE .13 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    COCAMIDOPROPYL BETAINE  
    UNDECETH-7  
    COCAMIDOPROPYLAMINE OXIDE  
    LAURAMINE OXIDE  
    EDETATE SODIUM  
    CITRIC ACID MONOHYDRATE  
    MAGNESIUM NITRATE  
    METHYLCHLOROISOTHIAZOLINONE  
    MAGNESIUM CHLORIDE  
    METHYLISOTHIAZOLINONE  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:11084-255-27 1000 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 07/20/2013
    Labeler - Deb USA, Inc. (607378015)
    Establishment
    Name Address ID/FEI Business Operations
    Deb USA, Inc. 607378015 manufacture(11084-255)
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