Label: PRO ADVANTAGE ANTIBACTERIAL - triclosan liquid 

  • Label RSS
  • NDC Code(s): 43128-128-03
  • Packager: NDC National Distribution & Contracting, 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 04/13

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

  • Pro Advantage Antibacterial Liquid Soap
  • Active Ingredient

    Triclosan, 0.3%

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  • Purpose

    Antiseptic Handwash

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  • Use

    Handwash to help reduce bacteria that potentially can cause disease.

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  • Warnings

    • For external use only

    Ask a doctor before use if you have

    • Deep wounds, animals bites, or serious burns.

    When using this product

    • Avoid contact with eyes. If this occurs, rinse thoroughly with water.

    Stop use and ask a doctor if

    • Irritation, itching or redness develops. If condition persists for more than 72 hours consult a doctor.

    Keep out of reach of children.

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

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  • Directions

    Wet hands, apply soap, lather for 30 seconds, and rinse hands thoroughly.

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  • Inactive Ingredients

    Water, Sodium Laureth Sulfate, Cocamine Oxide, Sodium Chloride, Cocamidopropyl Betaine, Propylene Glycol, DMDM Hydantoin, Fragrance, FDandC Yellow 5, FDandC Red 40

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  • REF: P778128 NDC 43128-108-03

    Made in China
    www.ProAdvantagebyNDC.com

    Manufactured for NDC, Inc.
    407 New Sanford Road, La Vergne, TN 37086

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  • Product Label
  • INGREDIENTS AND APPEARANCE
    PRO ADVANTAGE ANTIBACTERIAL 
    triclosan liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:43128-128
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TRICLOSAN (TRICLOSAN) TRICLOSAN 3 mg  in 0.001 L
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    SODIUM LAURETH-3 SULFATE  
    COCAMINE OXIDE  
    SODIUM CHLORIDE  
    COCAMIDOPROPYL BETAINE  
    PROPYLENE GLYCOL  
    DMDM HYDANTOIN  
    FD&C YELLOW NO. 5  
    FD&C RED NO. 40  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:43128-128-03 3.8 L in 1 JUG
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 04/24/2013
    Labeler - NDC National Distribution & Contracting, Inc. (009831413)
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