SAFEWAY HOME LEMON SCENT (TRICLOSAN) SOAP [SUN PRODUCTS CORPORATION]

SAFEWAY HOME LEMON SCENT (TRICLOSAN) SOAP [SUN PRODUCTS CORPORATION]
PDF | XML

NDC 63691-012-10
Set ID 55ef1be8-7ec4-4673-b54d-d727082d36a1
Category HUMAN OTC DRUG LABEL
Packager Sun Products Corporation
Generic Name
Product Class
Product Number
Application Number PART333E
  • 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, TEA-Dodecylbenzenesulfonate, Sodium Laureth Sulfate, Sodium Methyl 2-Sulfopalmitate, Lauramine Oxide, Sodium Lauryl Sulfate, Alcohol Denat., Disodium 2-Sulfopalmitate, Methyl Palmitate, Fragrance, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Benzophenone-4, Yellow No. 5

    Questions? 1-888-723-3929

  • PRINCIPAL DISPLAY PANEL

    front label

    LBLFR

    back label

    LBLBK

  • INGREDIENTS AND APPEARANCE
    SAFEWAY HOME LEMON SCENT  
    triclosan soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63691-012
    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)  
    TRIETHANOLAMINE DODECYLBENZENESULFONATE (UNII: 8HM7ZD48HN)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    ALCOHOL (UNII: 3K9958V90M)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    DISODIUM 2-SULFOPALMITATE (UNII: VS9295575T)  
    METHYL PALMITATE (UNII: DPY8VCM98I)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    SULISOBENZONE (UNII: 1W6L629B4K)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63691-012-10709 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E07/01/2013
    Labeler - Sun Products Corporation (070931480)

Related Drugs