Label: ALGONQUIN HANCLEAN FOAM- benzalkonium chloride soap

  • NDC Code(s): 65585-520-01, 65585-520-02
  • Packager: Whisk Products, Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 8, 2023

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  • ​Active Ingredient

    Benzalkonium Chloride 0.1%

  • ​Purpose

    Skin Antimicrobial

  • ​Uses

    • Reduces amount of bacteria on hands
    • Recommended for repeated use
  • ​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 or redness develops, 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.

  • ​Directions

    • Pump a small amount of foam into palm of hand.
    • Rub thoroughly over all surfaces of both hands for fifteen seconds.
    • Rinse with potable water.

  • ​Inactive Ingredients

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

  • PRINCIPAL DISPLAY PANEL

    4 L Kwik-Klick Cartridge Label

  • INGREDIENTS AND APPEARANCE
    ALGONQUIN HANCLEAN FOAM 
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65585-520
    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
    WATER (UNII: 059QF0KO0R)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    Product Characteristics
    Colorwhite (colorless, water-white (dispensed as a white foam)) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65585-520-014000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/29/2020
    2NDC:65585-520-028 in 1 BOX04/29/2020
    21000 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/29/2020
    Labeler - Whisk Products, Inc. (834270639)
    Establishment
    NameAddressID/FEIBusiness Operations
    Whisk Products, Inc.834270639manufacture(65585-520)
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