Label: NATURAL EXTENSIONS ANTIBACTERIAL FOAMING HAND- benzalkonium chloride soap

  • NDC Code(s): 66975-104-01, 66975-104-02
  • Packager: Benco Dental
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 28, 2023

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  • Active Ingredient

    Benzalkonium Chloride 0.1%

  • Purpose

    Skin Antimicrobial

  • Use

    For handwashing to decrease bacteria on the skin

  • Warnings

    For external use only.

    Do not use in eyes. In case of eye contact, flush thoroughly with water and seek medical attention.

    Stop use and ask a doctor if irritation and redness develop and 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.

  • Directions

    • Wet hands, apply liberal amount of product.
    • Rub hands together for 30 seconds.
    • Rinse thoroughly.
  • Other Information

    Keep from freezing

  • Inactive Ingredients

    Water, Lauramine Oxide, Glycerin, PEG-120 Methyl Glucose Dioleate, Fragrance

  • Questions or comments?

    1-800-GO-BENCO www.benco.com

  • PRINCIPAL DISPLAY PANEL

    Product Label - 1 gallon Short Neck Bottle

  • INGREDIENTS AND APPEARANCE
    NATURAL EXTENSIONS ANTIBACTERIAL FOAMING HAND 
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66975-104
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Colorwhite (water white - colorless, dispensed as white foam) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66975-104-013785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/15/2018
    2NDC:66975-104-02530 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product11/15/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)11/15/2018
    Labeler - Benco Dental (015108087)
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