Label: WHISKCARE 377 FREE- benzalkonium chloride solution

  • NDC Code(s): 65585-527-01, 65585-527-02, 65585-527-03
  • 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

    Antimicrobial

  • ​Uses

    • For hand sanitizing to decrease bacteria on the skin
    • 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.
    • Rub hands together briskly until dry.
  • ​Inactive Ingredients

    Water, Cocamidopropyl PG-Dimonium Chloride Phosphate, Dihydroxyethyl Cocamine Oxide, Acetamidoethoxyethanol, Citric Acid

  • PRINCIPAL DISPLAY PANEL

    1 Gallon Product Label

  • INGREDIENTS AND APPEARANCE
    WHISKCARE 377  FREE
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65585-527
    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)  
    COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)  
    ACETAMIDOETHOXYETHANOL (UNII: LVX2APC4XR)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Product Characteristics
    Colorwhite (water white - colorless, dispensed as a white foam) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65585-527-018 in 1 BOX10/05/2023
    11000 mL in 1 BAG; Type 0: Not a Combination Product
    2NDC:65585-527-023785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/05/2023
    3NDC:65585-527-034 in 1 BOX02/22/2024
    31000 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)10/05/2023
    Labeler - Whisk Products, Inc. (834270639)
    Establishment
    NameAddressID/FEIBusiness Operations
    Whisk Products, Inc.834270639manufacture(65585-527)
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