Label: SCOTT CLEAR ANTIBACTERIAL SKIN CLEANSER- 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 October 7, 2014

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Triclosan 0.25%

  • 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
  • Inactive Ingredients

    Water, Sodium Laureth Sulfate, Sodium Chloride, Cocamidopropyl Beteine, Glycerin, Propylene Glycol, Frangrance, DL-Panthenol, Aloe Barbadensis Leaf Juice, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone, Cocamide DEA.

  • Questions?

    1-888-346-4652

  • SPL UNCLASSIFIED SECTION

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

    Distributed in Canada by Kimberly-Clark Inc., Mississauga, Ontario L5B 3Y5

  • PRINCIPAL DISPLAY PANEL - 500 mL Carton

    92517

    Scott*
    BRAND

    Clear Antibacterial Skin Cleanser

    Triclosan 0.25%

    DIN: 02369818

    500 mL (16.9 fl oz)

    PRINCIPAL DISPLAY PANEL - 500 mL Carton
  • INGREDIENTS AND APPEARANCE
    SCOTT CLEAR ANTIBACTERIAL SKIN CLEANSER 
    triclosan solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-205
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X) Triclosan0.25 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    Sodium Laureth-3 Sulfate (UNII: BPV390UAP0)  
    Sodium Chloride (UNII: 451W47IQ8X)  
    Cocamidopropyl Betaine (UNII: 5OCF3O11KX)  
    Coco Diethanolamide (UNII: 92005F972D)  
    Glycerin (UNII: PDC6A3C0OX)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    Panthenol (UNII: WV9CM0O67Z)  
    Aloe Vera Leaf (UNII: ZY81Z83H0X)  
    Citric Acid Monohydrate (UNII: 2968PHW8QP)  
    Methylchloroisothiazolinone (UNII: DEL7T5QRPN)  
    Methylisothiazolinone (UNII: 229D0E1QFA)  
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55118-205-05500 mL in 1 BAG; Type 0: Not a Combination Product
    2NDC:55118-205-08800 mL in 1 BAG; Type 0: Not a Combination Product
    3NDC:55118-205-101000 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart333E03/01/2012
    Labeler - Kimberly-Clark Corporation (006072136)
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