Label: E2 SANITIZING HAND soap

  • NDC Code(s): 50865-017-03, 50865-017-07, 50865-017-09, 50865-017-41, view more
    50865-017-65, 50865-017-67
  • Packager: KUTOL PRODUCTS COMPANY
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 18, 2024

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  • Active Ingredient

    Benzalkonium Chloride 0.13% w/w

  • Purpose

    Antibacterial Agent

  • Uses

    For handwashing to help reduce bacteria on the skin that could cause disease.

  • Warnings

    For external use only. Avoid contact with eyes. If contact occurs, flush with water.

    Stop use and ask a doctor if, in rare instances, redness or irritation develops and persists for more than 72 hours.

    Keep out of reach of children. If swallowed, contact a physician or poison control center.

  • Directions

    To decrease bacteria on skin, apply small amount, covering hands with product for 30 seconds. Add water, lather, rinse.

  • Inactive Ingredients

    Water, Cocamidopropyl PG-Dimonium Chloride Phosphate, Cocamidopropyl Betaine, PEG-6 Cocamide, Hydroxyethyl Cellulose, Laurtrimonium Chloride, Iodopropynyl Butylcarbamate, Methylisothiazolinone.

  • QUESTIONS

    Kutol Product Co.
    Cincinnati, OH 45241
    www.Kutol.com

  • 1703 label

    1703 label

  • 1707 label

    1707 label

  • 1709 label

    1709 label

  • 1765 label

    1765 label

  • 1767 label

    1767 label

  • INGREDIENTS AND APPEARANCE
    E2 SANITIZING HAND 
    e2 sanitizing hand soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50865-017
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.003 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    PEG-6 COCAMIDE (UNII: YZ6NLA4O1E)  
    HYDROXYETHYL CELLULOSE (280 MPA.S AT 2%) (UNII: 12VCE9HR9E)  
    LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50865-017-03209000 mL in 1 DRUM; Type 0: Not a Combination Product09/15/2015
    2NDC:50865-017-074000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/15/2015
    3NDC:50865-017-094000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/15/2015
    4NDC:50865-017-65800 mL in 1 BAG; Type 0: Not a Combination Product09/15/2015
    5NDC:50865-017-672000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/15/2015
    6NDC:50865-017-411000 mL in 1 BAG; Type 0: Not a Combination Product09/15/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)09/15/2015
    Labeler - KUTOL PRODUCTS COMPANY (004236139)
    Registrant - Kutol Products Company (004236139)
    Establishment
    NameAddressID/FEIBusiness Operations
    Kutol Products Company, Inc.004236139manufacture(50865-017)
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