Label: ZOGICS ANTIBACTERIAL HAND- chloroxylenol soap

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 15, 2024

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Chloroxylenol 0.1%

  • PURPOSE

    Antiseptic Handwashing

  • USES

    Handwash to help decrease bacteria on the skin.

  • WARNINGS

    For external use only.
    Do not use in the eyes. In case of contact, immediately flush eyes with water.

  • ASK DOCTOR

    Stop use and ask a doctor if irritation or rash appears and lasts.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control Center right away.

  • DIRECTIONS

    Apply a small amount, covering hands with product for 30 seconds. Lather and rinse.
    Children under 6 years of age should be supervised when using this product.

  • INACTIVE INGREDIENTS

    Water, Sodium C14-16 Olefin Sulfonate, Sodium Chloride, Sodium Laureth Sulfate, Cocamidopropyl Betainer, Sodium Sulfate, Propylene Glycol, Glycerin, Sodium Lauryl Sulfate, Propanediol, Glycol Distearate, Tetrasodium EDTA, Fragrance, Styrene/Acrylates Copolymer, Dibromocyanoacetamide, Methylisothiazolinone, Methylchloroisothiazolinone

  • PRINCIPAL DISPLAY PANEL

    Principal Display Panel

  • INGREDIENTS AND APPEARANCE
    ZOGICS ANTIBACTERIAL HAND 
    chloroxylenol soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72202-301
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL1 g  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    HEXAMETHYLINDANOPYRAN (UNII: 14170060AT)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    DIBROMOCYANOACETAMIDE (UNII: 7N51QGL6MJ)  
    ALLYL AMYL GLYCOLATE (UNII: EMX89K493E)  
    GLYCOL DISTEARATE (UNII: 13W7MDN21W)  
    .GAMMA.-NONALACTONE (UNII: I1XGH66S8P)  
    ALLYL HEXANOATE (UNII: 3VH84A363D)  
    ETHYL CAPROATE (UNII: FLO6YR1SHT)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    SODIUM SULFATE (UNII: 0YPR65R21J)  
    VANILLIN (UNII: CHI530446X)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    EDETATE SODIUM TETRAHYDRATE (UNII: L13NHD21X6)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72202-301-413.78 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/15/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)03/15/2024
    Labeler - Zogics, LLC (796321870)