Label: KROGER ANTIBACTERIAL ORANGE SCENT HAND- chloroxylenol soap

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 6, 2023

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

View All Sections
  • Drug Facts

  • Active ingredient

    Chloroxylenol 0.3%

  • Purpose

    Antibacterial

  • Use

    for handwashing to decrease bacteria on the skin

  • Warnings

    For external use only: hands only

    When using this product • do not get into eyes. If contact occurs, rinse eyes thoroughly with water.

    Stop use and ask a doctor if • irritation and redness develop • 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

    • wet hands and forearms. • apply palmful to hands and forearms. • scrub thoroughly for 30 seconds and rinse.

  • Inactive ingredients

    water, sodium laureth sulfate, sodium lauryl sulfate, lauramine oxide, sodium xylenesulfonate, propylene glycol, citric acid, orange 4, fragrance, methylchloroisothiazolinone, methylisothiazolinone. Contains fragrance allergen.

  • SPL UNCLASSIFIED SECTION

    Kroger®

    COMPARE TO DAWN® ULTRA ANTIBACTERIAL

    2X CLEANING POWER VERSUS NON-CONCENTRATED DISH SOAPS

    GREASE CLEANING

    ULTRA CONCENTRATED DISH SOAP

    Our Brands. Our Guarantee.
    Love It or Your Money Back.

    www.kroger.com

    For More Ingredient Information, Visit www.kroger.com or call 800-632-6900

    Do not add bleach. Not for use in dishwashers.

    Contains surfactants

    Phosphate Free

    DISTRIBUTED BY THE KROGER CO.

    CINCINNATI, OHIO 45202

    *Dawn® is a registered trademark of The Procter and Gamble Company, Cincinnati, OH 45202. The Procter and Gamble Company is not affiliated with The Kroger Co. or this product.

  • Packaging

    Korex-006

  • INGREDIENTS AND APPEARANCE
    KROGER ANTIBACTERIAL ORANGE SCENT HAND 
    chloroxylenol soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73487-006
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    SODIUM XYLENESULFONATE (UNII: G4LZF950UR)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    D&C ORANGE NO. 4 (UNII: Q1LIY3BO0U)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73487-006-01828 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/202202/01/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/01/202202/01/2025
    Labeler - Korex Chicago LLC (792133147)
    Establishment
    NameAddressID/FEIBusiness Operations
    Korex Chicago LLC792133147manufacture(73487-006)
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!