Label: SCOTT ANTIBACTERIAL- triclosan solution

  • 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 November 12, 2014

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Triclosan Liquid 0.5% w/w

  • Purpose

    Antiseptic

  • Use

    For handwashing to decrease bacteria on the skin.

  • Warnings

    For External Use Only.

    When using this product avoid contact with eyes; in case of contact, flush eyes with water.

    Stop use & ask a doctor if irritation or redness develops and persists.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

  • Directions

    Wet hands and apply a palmful to hands. Scrub thoroughly for 15-20 seconds. Rinse and dry thoroughly.

  • Other Information

    • Report serious side effects from this product to 1-877-561-6587
  • Ingredients

    Water, Propylene Glycol, Sodium Citrate, Sodium Cumenesulfonate, Sodium Laureth Sulfate, Citric Acid, Cocamidopropyl Betaine, PEG-7 Glyceryl Cocoate, Fragrance, Disodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone

  • Questions?

    1-888-346-4652

  • SPL UNCLASSIFIED SECTION

    Distributed in the U.S. by Kimberly-Clark Global Sales, LLC,
    Roswell, GA 30076-2199

  • PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label

    Kimberly-Clark
    PROFESSIONAL*

    Scott®
    BRAND

    Antibacterial
    Foam Soap

    Intended for use in restrooms
    and non-processing areas only.

    Triclosan Liquid 0.5%

    1 Liter
    (33.8 fl oz)

    NDC: 055118-425-10

    Principal Display Panel - 1 Liter Bottle Label
  • INGREDIENTS AND APPEARANCE
    SCOTT ANTIBACTERIAL 
    triclosan solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-425
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X) Triclosan5 g  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    Sodium Citrate (UNII: 1Q73Q2JULR)  
    Sodium Cumenesulfonate (UNII: 5798KA13PG)  
    Sodium Laureth-3 Sulfate (UNII: BPV390UAP0)  
    Citric Acid Monohydrate (UNII: 2968PHW8QP)  
    Cocamidopropyl Betaine (UNII: 5OCF3O11KX)  
    Edetate Disodium (UNII: 7FLD91C86K)  
    Methylchloroisothiazolinone (UNII: DEL7T5QRPN)  
    Methylisothiazolinone (UNII: 229D0E1QFA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55118-425-101 L in 1 CARTRIDGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart333E02/01/2011
    Labeler - Kimberly-Clark Corporation (006072136)
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