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
  • DEA Schedule: None

Drug Label Information

Updated February 22, 2024

If you are a consumer or patient please visit this version.

View All Sections
  • 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)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!