Label: ACTION CHEMICAL ANTIBAC CLEAR- triclosan liquid

  • 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 5, 2017

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

  • Active ingredient

    Triclosan, 0.30%

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  • Purpose

    Antibacterial

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  • Uses

    For hand washing to reduce bacteria on the skin

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  • Warnings

    For external use only

    When using this product

    avoid contact with eyes. In case of eye contact, flush with water.

    Keep out of reach of children.

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

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  • Directions

    Apply foaming cleanser to dry hands

    Rub hands together to spread lather

    Wash for 15-20 seconds

    Rinse and dry hands thoroughly

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  • Inactive ingredients

    Water, Sodium Laureth Sulfate, Propylene Glycol, PEG-7 Glyceryl Cocoate, Glycerin, Cocamidopropyl Betaine, 2-Bromo-2-nitropropane-1,3-diol, Fragrance, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone.

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  • PRINCIPAL DISPLAY PANEL

    Clear Foaming Antimicrobial Soap

    Ideal for use where antimicrobial action is desired.

    A high-quality, foam soap that is 99.99% effective against common bacteria.

    Action Chemical Inc.

    Proudly made in the USA for: Action Chemical, Inc.

    Memphis, TN 38101

    Phone: 901-522-8783

    Phone: 877-422-8783

    www.actionchemical.com

    57151

    1 Liter

    33.8 Fluid Ounces

    Rev. 09-13

    57151-ActionChem-V7.jpg

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  • INGREDIENTS AND APPEARANCE
    ACTION CHEMICAL ANTIBAC CLEAR 
    triclosan liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:11084-147
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 0.30 mg  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    BRONOPOL (UNII: 6PU1E16C9W)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:11084-147-27 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/12/2013 08/01/2020
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 09/12/2013 08/01/2020
    Labeler - Deb USA, Inc. (607378015)
    Establishment
    Name Address ID/FEI Business Operations
    Deb USA, Inc. 078805627 manufacture(11084-147)
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