Label: WHISKCARE 357- benzalkonium chloride soap

  • NDC Code(s): 65585-557-01, 65585-557-02, 65585-557-03, 65585-557-04, view more
    65585-557-05, 65585-557-06, 65585-557-07, 65585-557-08, 65585-557-09
  • Packager: Whisk Products, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 22, 2024

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  • Active Ingredient

    Benzalkonium Chloride 0.1%

  • Purpose

    Skin Antimicrobial

  • Uses

    • Reduces amount of bacteria on hand
    • 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 at least fifteen seconds.
    • Rinse with potable water.
  • Inactive Ingredients

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

  • PRINCIPAL DISPLAY PANEL

    1 Gallon Product Label

  • INGREDIENTS AND APPEARANCE
    WHISKCARE 357 
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65585-557
    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
    GLYCERIN (UNII: PDC6A3C0OX)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    WATER (UNII: 059QF0KO0R)  
    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:65585-557-0150 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/25/2020
    2NDC:65585-557-026 in 1 BOX03/25/202009/30/2024
    2500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    3NDC:65585-557-038 in 1 BOX03/25/2020
    31000 mL in 1 BAG; Type 0: Not a Combination Product
    4NDC:65585-557-046 in 1 BOX03/25/2020
    41750 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    5NDC:65585-557-053785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/25/2020
    6NDC:65585-557-06208198 mL in 1 DRUM; Type 0: Not a Combination Product03/25/2020
    7NDC:65585-557-076 in 1 BOX11/20/202012/01/2022
    7850 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    8NDC:65585-557-084 in 1 BOX03/04/202112/31/2022
    81000 mL in 1 BAG; Type 0: Not a Combination Product
    9NDC:65585-557-094 in 1 BOX02/22/2024
    91000 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)03/25/2020
    Labeler - Whisk Products, Inc. (834270639)
    Establishment
    NameAddressID/FEIBusiness Operations
    Whisk Products, Inc.834270639manufacture(65585-557)
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