PUBLIX ULTRADISH DETERGENT (TRICLOSAN) SOAP [SUN PRODUCTS CORPORATION]

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  • PUBLIX ULTRADISH DETERGENT (TRICLOSAN) SOAP [SUN PRODUCTS CORPORATION]

PUBLIX ULTRADISH DETERGENT (TRICLOSAN) SOAP [SUN PRODUCTS CORPORATION]
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NDC 63691-014-10
Set ID 4ce4c100-b75a-478b-9fda-756a04ccdbc3
Category HUMAN OTC DRUG LABEL
Packager Sun Products Corporation
Generic Name
Product Class
Product Number
Application Number PART333E
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  • ACTIVE INGREDIENT

    Active ingredient

    Triclosan 0.10%

    Use helps fight germs on hands when used as a hand soap

    For external use only

    Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.  In case of eye contact, rinse thoroughly with water.

    Directions wash hands and rinse

    Antibacterial hand soap

    Inactive ingredients Water, Sodium Lauryl Sulfate, Sodium Laureth Sulfate, Lauramine Oxide, Sodium Dodecylbenzenesulfonate, Sodium Xylene Sulfonate, Alcohol Denat., Fragrance, Sodium Citrate, Methylchloroisothiazolinone, Methylisothiazolinone, Benzophenone-4, Red No. 33, Yellow No. 5

    Questions? 1-800-776-6702

  • PRINCIPAL DISPLAY PANEL

    front label

    LBLFR

    back label

    LBLBK

  • INGREDIENTS AND APPEARANCE
    PUBLIX ULTRADISH DETERGENT  
    triclosan soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63691-014
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN0.1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    ALCOHOL (UNII: 3K9958V90M)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    SODIUM XYLENESULFONATE (UNII: G4LZF950UR)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    SULISOBENZONE (UNII: 1W6L629B4K)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63691-014-10709 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E06/01/2013
    Labeler - Sun Products Corporation (070931480)
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