Label: GENUINE JOE ANTIBACTERIAL- pcmx soap

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

Drug Label Information

Updated November 10, 2023

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  • Active Ingredient

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

  • Inactive Ingredients

    Water, Cocamidopropyl Betaine, Sodium Lauryl Sulfate, Sodium Laureth-3 Sulfate, Sodium Chloride, Propylene glycol, Propanediol, Fragrance, Methylchloroisothiazolinone, Methylisothiazolinone, Yellow 5, and Red 40.

  • PRINCIPAL DISPLAY PANEL

    Principal Display Panel

  • INGREDIENTS AND APPEARANCE
    GENUINE JOE ANTIBACTERIAL 
    pcmx soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62832-701
    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 CHLORIDE (UNII: 451W47IQ8X)  
    EUGENOL (UNII: 3T8H1794QW)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
    WATER (UNII: 059QF0KO0R)  
    CINNAMALDEHYDE (UNII: SR60A3XG0F)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    Product Characteristics
    Colororange (Clear) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62832-701-413.78 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/09/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/09/2021
    Labeler - S.P. Richards Company (007976384)
    Registrant - Midlab, Inc. (047371463)
    Establishment
    NameAddressID/FEIBusiness Operations
    Midlab, Inc.047371463manufacture(62832-701)
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