Label: COMPLIANCE DISHWASHING LIQUID AND ANTIBACTERIAL HAND- pcmx soap

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

Drug Label Information

Updated January 4, 2024

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  • Active Ingredient

    Chloroxylenol 0.1%

  • Purpose

    Antiseptic Handwashing

  • Uses

    • Dishwashing concentrate and antimicrobial hand soap.

  • 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. Add water, lather and rinse.
    • Children under 6 years of age should be supervised when using this product.

  • Inactive Ingredients

    Sodium Lauryl Sulfate (68585-47-7), Sodium Chloride (7647-14-5), Lauramine Oxide (1643-20-5), Propylene Glycol (57-55-6), Cocamidopropyl Hydroxysultaine (68139-30-0), Fragrance (Proprietary), Propanediol (26264-14-2), Sodium Polyitaconate (26099-89-8), 2-Bromo-2-Nitropropane-1,3-Diol (52-51-7), Dibromocyanoacetamide (10222-01-2), Methylchloroisothiazolinone (26172-55-4), Methylisothiazolinone (2682-20-40), Yellow 5 (1934-21-0), and Red 40 (25956-17-6).

  • PRINCIPAL DISPLAY PANEL

    Principal Display Panel

  • INGREDIENTS AND APPEARANCE
    COMPLIANCE DISHWASHING LIQUID AND ANTIBACTERIAL HAND 
    pcmx soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59723-101
    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
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SODIUM POLYITACONATE (2800 MW, PHOSPHATE TERMINATED) (UNII: G7SW5QN7TT)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    EUGENOL (UNII: 3T8H1794QW)  
    WATER (UNII: 059QF0KO0R)  
    CINNAMALDEHYDE (UNII: SR60A3XG0F)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    DIBROMOCYANOACETAMIDE (UNII: 7N51QGL6MJ)  
    BRONOPOL (UNII: 6PU1E16C9W)  
    COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)  
    Product Characteristics
    Colororange (Clear) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59723-101-413.78 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/05/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)08/05/2022
    Labeler - Royal Paper Corp. (148594229)
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