Label: DELUXE ALL-PURPOSE- 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 April 2, 2012

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  • Active Ingredient

    Drug Facts  Active Ingredients  Triclosan 0.2 %

  • Purpose

    Purpose  Handwash

  • Keep Out of Reach of Children

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

  • Uses

    Antimicrobial handwash.

  • Warnings

    Warnings - For external use only.

    When using this product - Keep out of eyes. In case of contact with eyes, flush thoroughly with water.

  • Directions

    Directions - Dispense a small amount of soap into hands or on a washcloth. Work up a lather and rinse with water.

  • Inactive Ingredients

    Inactive Ingredients - As-40, Cd-6, Color, Dantogard, Propylene Glycol, Water.

  • Package Label

    Johnson Labs   DELUXE ALL-PURPOSE LIQUID HAND SOAP

    This state-of-the-art hand soap was developed to be used in industries, schools, offices or wherever people need a high quality hand soap. This product can also be used as a hair and body shampoo and clothes wash.

    1 Gallon (3.78L)  made in U.S.A.  Johnson Labs, Inc. Troy, AL 36081  334-566-9152  800-473-9152

    Deluxe All-Purpose Liquide Hand Soap

  • INGREDIENTS AND APPEARANCE
    DELUXE ALL-PURPOSE  
    triclosan liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59854-301
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN7.57 mL  in 3.78 L
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    COCO DIETHANOLAMIDE (UNII: 92005F972D)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59854-301-013.78 L in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/01/2000
    Labeler - Johnson Labs, Inc. (805806742)
    Registrant - Johnson Labs, Inc. (805806742)
    Establishment
    NameAddressID/FEIBusiness Operations
    Johnson Labs, Inc.805806742manufacture
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