Label: NORTH WOODS DERMA FOAM E-2- benzalkonium chloride soap

  • NDC Code(s): 53125-817-29
  • Packager: Superior Chemical Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 18, 2024

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  • ACTIVE INGREDIENT

    ​Active Ingredient

    Benzalkonium Chloride 0.13%

  • INDICATIONS & USAGE

    Uses

    • For handwashing to decrease the bacteria on the skin.
    • Recommended for repeated use.
  • WARNINGS

    Warnings

    • For external use only.
    • When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.
    • Stop use and ask a doctor If irritation persists or redness deelops, or if condition persists for more than 72 hours.
    • Keep out of reach of children.
    • If swallowed, get medical help or contact a Poison Control Center right away.
  • DOSAGE & ADMINISTRATION

    Directions

    • ​Read the entire label before using this product.
    • ​Dispense 2 pumps of product onto palm of hand and scrub thoroughly over all surfaces of both hands for 15 seconds. Rinse with clean water.
  • INACTIVE INGREDIENT

    Inactive Ingredients

    ​Water, coco-glucoside, laurtrimonium chloride, cocamidopropylamine oxide, citric acid.

  • Superior Derma Foam E2

    Purpose

    Antimicrobial

  • Superior Derma Foam E2

    KEEP OUT OF REACH OF CHILDREN

  • Superior Derma Foam E2

    71729-00 Superior Derma Foam

    71729-00 Superior Derma Foam E2

  • INGREDIENTS AND APPEARANCE
    NORTH WOODS DERMA FOAM E-2 
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53125-817
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    ALCOHOL (UNII: 3K9958V90M)  
    TETRASODIUM EDTA (UNII: MP1J8420LU)  
    WATER (UNII: 059QF0KO0R)  
    LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
    CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53125-817-291000 mL in 1 BAG; Type 0: Not a Combination Product09/15/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)09/15/2016
    Labeler - Superior Chemical Corporation (023335086)
    Registrant - Betco corporation, Ltd. (024492831)
    Establishment
    NameAddressID/FEIBusiness Operations
    Betco Corporation, Ltd.005050158manufacture(53125-817) , label(53125-817) , pack(53125-817)