Label: SIGNATURE HOME AB ORANGE- chloroxylenol 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 June 29, 2016

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  • Dishwashing Liquid & Antibacterial Hand Soap

    ULTRA Concentrated

    orange scent

  • Active Ingredient

    Chloroxylenol 0.30%

  • Purpose

    Antibacterial hand soap

  • Use

    for handwashing to decrease bacteria on the skin

  • Warnings

    For external use only

    .

  • Keep out of reach of children

    In case of accidental ingestion, drink a glass of water to dilute. If eye contact occurs, rinse thoroughly with water.

  • Directions

    wet hands and forearms. Apply 5 ml or palmful to hands and forearms. Scrub thoroughly for 30 sec. and rinse.

  • Inactive ingredients

    Water, Sodium Laureth Sulfate, Sodium Didecylbenzenesulfonate, Sodium Chloride, Alcohol Denat., Sodium Xylenesulfonate, Sodium Lauryl Sulfate, Tetrasodium EDTA, Benzisothiazolinone, Methylisothiazolinone, Methylchloroisothiazolinone, Fragrance, FD&C Yello No. 5, D&C Red No. 33

  • Questions?

    Questions? 1-888-723-3929

  • Signature Home Orange AB-page-001.jpg

    Signature Home Orange AB

  • INGREDIENTS AND APPEARANCE
    SIGNATURE HOME AB ORANGE 
    chloroxylenol soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63691-027
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM XYLENESULFONATE (UNII: G4LZF950UR)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    ALCOHOL (UNII: 3K9958V90M)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    WATER (UNII: 059QF0KO0R)  
    BENZISOTHIAZOLINONE (UNII: HRA0F1A4R3)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorORANGEImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63691-027-10709 mL in 1 BOTTLE; Type 0: Not a Combination Product04/30/2016
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E04/30/2016
    Labeler - Sun Products Corporation (070931480)
    Registrant - Safeway (009137209)
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