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Scott Antibacterial Foam (Kimberly-Clark Corporation)

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SOLUTION 1 L in 1 CARTRIDGE (55118-425-10) Label Information

Complete Scott Antibacterial Foam Information

  • 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 Type HUMAN OTC DRUG Item Code (Source) NDC:55118-425
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X) Triclosan 5 g  in 1 L
    Inactive Ingredients
    Ingredient Name Strength
    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 Code Package Description Marketing Start Date Marketing End Date
    1 NDC:55118-425-10 1 L in 1 CARTRIDGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part333E 02/01/2011
    Labeler - Kimberly-Clark Corporation (006072136)