Label: PRO ADVANTAGE ANTIBACTERIAL- triclosan liquid

  • NDC Code(s): 43128-128-03
  • Packager: NDC National Distribution & Contracting, Inc.
  • Category: HUMAN OTC DRUG LABEL

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 March 15, 2023

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  • Pro Advantage Antibacterial Liquid Soap


  • Active Ingredient

    Triclosan, 0.3%

  • Purpose

    Antiseptic Handwash

  • Use

    Handwash to help reduce bacteria that potentially can cause disease.

  • 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.

  • Directions

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

  • Inactive Ingredients

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

  • REF: P778128 NDC 43128-108-03

    Made in China
    www.ProAdvantagebyNDC.com

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

  • Product Label

    AntibacterialLiquidSoap

  • INGREDIENTS AND APPEARANCE
    PRO ADVANTAGE ANTIBACTERIAL 
    triclosan liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43128-128
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN3 mg  in 0.001 L
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
    COCAMINE OXIDE (UNII: QWA2IZI6FI)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43128-128-033.8 L in 1 JUG; Type 0: Not a Combination Product04/24/2013
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E04/24/2013
    Labeler - NDC National Distribution & Contracting, Inc. (009831413)
    Establishment
    NameAddressID/FEIBusiness Operations
    Dukal088520668manufacture(43128-128)
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