Label: EXCHANGE SELECT ULTRA CITRUS SCENT- triclosan soap

  • 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 December 30, 2014

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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 Dodecylbenzenesulfonate, Sodium Laureth Sulfate, Sodium Methyl 2-Sulfopalmitate, Magnesium Sulfate, Sodium Xylenesulfonate, Alcohol Denat., Fragrance, Disodium 2-Sulfopalmitate, Methyl Palmitate, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Benzophenone-4, D&C Orange No. 4, Sodium Citrate

    Questions? 1-800-776-6702

  • PRINCIPAL DISPLAY PANEL

    front label

    LBLFR

    back label

    LBLBK

  • INGREDIENTS AND APPEARANCE
    EXCHANGE SELECT ULTRA CITRUS SCENT 
    triclosan soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63691-024
    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 LAURETH SULFATE (UNII: BPV390UAP0)  
    MAGNESIUM SULFATE (UNII: DE08037SAB)  
    SODIUM XYLENESULFONATE (UNII: G4LZF950UR)  
    ALCOHOL (UNII: 3K9958V90M)  
    DISODIUM 2-SULFOPALMITATE (UNII: VS9295575T)  
    METHYL PALMITATE (UNII: DPY8VCM98I)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    SULISOBENZONE (UNII: 1W6L629B4K)  
    D&C ORANGE NO. 4 (UNII: Q1LIY3BO0U)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63691-024-12591 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E07/01/2014
    Labeler - Sun Products Corporation (070931480)
    Registrant - Military Exchange (827856670)
    Establishment
    NameAddressID/FEIBusiness Operations
    Sun Products Corporation - Salt Lake City096752865manufacture(63691-024)
    Establishment
    NameAddressID/FEIBusiness Operations
    Sun Products Corporation - Bowling Green809709314manufacture(63691-024)
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