Label: WHISKCARE 367- chloroxylenol soap

  • NDC Code(s): 65585-568-01, 65585-568-02, 65585-568-03, 65585-568-04, view more
    65585-568-05, 65585-568-06, 65585-568-07, 65585-568-08
  • Packager: Whisk Products, Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated February 22, 2024

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  • Active Ingredient

    Chloroxylenol 0.75% w/w

  • Purpose

    Skin Antimicrobial

  • Use

    reduces amount of bacteria on hands

  • Warnings

    For external use only. Do not use in eyes.

    Discontinue use if irritation and redness develop. If condition persists for more than 72 hours, consult a physician.

    Not for use on children under six months of age.

    For institutional and professional use only.

  • Directions

    • Wet hands and forearms.
    • Apply a small amount (5 mL) or palmful to hands and forearms.
    • Scrub thoroughly for at least fifteen seconds.
    • Rinse completely and dry.
  • Inactive Ingredients

    Water, Propylene Glycol, TEA-Lauryl Sulfate, Lauramide DEA, Fragrance, DMDM Hydantoin, Yellow 5, Blue 1

  • PRINCIPAL DISPLAY PANEL

    Case Label - 8 x 1000 mL Bags

  • INGREDIENTS AND APPEARANCE
    WHISKCARE 367 
    chloroxylenol soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65585-568
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL7.5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    LAURIC DIETHANOLAMIDE (UNII: I29I2VHG38)  
    WATER (UNII: 059QF0KO0R)  
    TRIETHANOLAMINE LAURYL SULFATE (UNII: E8458C1KAA)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Product Characteristics
    Colorgreen (green, dispensed as a white foam) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65585-568-0159 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/06/2007
    2NDC:65585-568-026 in 1 BOX12/06/200706/30/2023
    21750 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    3NDC:65585-568-033785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/06/2007
    4NDC:65585-568-044 in 1 BOX12/06/200710/09/2014
    44000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    5NDC:65585-568-056 in 1 BOX12/06/2007
    5500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    6NDC:65585-568-068 in 1 BOX12/06/2007
    61000 mL in 1 BAG; Type 0: Not a Combination Product
    7NDC:65585-568-073 in 1 BOX01/08/201001/03/2017
    71200 mL in 1 BAG; Type 0: Not a Combination Product
    8NDC:65585-568-084 in 1 BOX02/22/2024
    81000 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)12/06/2007
    Labeler - Whisk Products, Inc. (834270639)
    Establishment
    NameAddressID/FEIBusiness Operations
    Whisk Products, Inc.834270639manufacture(65585-568)
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