Label: DERMACEN ANTIMICROBIAL-P HAND- chloroxylenol liquid

  • NDC Code(s): 62654-231-01, 62654-231-14, 62654-231-37, 62654-231-92
  • Packager: Central Solutions Inc
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 9, 2024

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  • ACTIVE INGREDIENT

    Active Ingredients

    Chloroxylenol (PCMX) 0.95%


  • PURPOSE

    Purpose

    Antimicrobial

  • INDICATIONS & USAGE

    Uses

    An effective antimicrobial hand cleanser

    Kills and inhibits bacterial growth on hands

    Gentle cleansers leave hands clean and moisturized

    Reduces the possibility of cross contamination



  • WARNINGS

    Warnings

    For External Use Only

    When using this product

    Avoid contact with eyes

    Discontinue use if irritation occurs

    Keep out of reach of children.

  • DOSAGE & ADMINISTRATION

    Directions

    Use as you would any liquid hand soap.

    Wet hands with water, then apply a small amount of product to palm.

    Rub hands together vigorously for at least 15 seconds.

    Rinse and dry thoroughly.

  • INACTIVE INGREDIENT

    Inactive Ingredients

    Purified Water, Sodium Laureth Sulfate, Isopropyl Alcohol, Lauramide DEA, Sodium Chloride, Styrene/Acrylates Copolymer, Disodium EDTA, DMDM Hydantoin and Iodopropynyl Butylcarbamate, Sodium Hydroxide, Fragrance, Glycereth-26, Aloe Barbadensis Leaf Juice, Yellow 5, Blue 1

  • PRINCIPAL DISPLAY PANEL

    DermaCen

    Antimicrobial-P

    Hand Soap

    An antimicrobial lotionized

    hand soap containing Aloe Vera

    to decrease bacteria on the skin

    NET CONTENTS 8.5 ounces (251 mL)

    container label

  • INGREDIENTS AND APPEARANCE
    DERMACEN ANTIMICROBIAL-P HAND 
    chloroxylenol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62654-231
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.95 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    LAURIC DIETHANOLAMIDE (UNII: I29I2VHG38)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    GLYCERETH-26 (UNII: NNE56F2N14)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62654-231-14251 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/05/2018
    2NDC:62654-231-37532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/05/2018
    3NDC:62654-231-921250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/05/2018
    4NDC:62654-231-013785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/05/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/01/2001
    Labeler - Central Solutions Inc (007118524)
    Establishment
    NameAddressID/FEIBusiness Operations
    Central Solutions Inc007118524manufacture(62654-231)
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