Label: DIAL ADVANCED CLEAN ANTIBACTERIAL GOLD- benzalkonium chloride soap

  • NDC Code(s): 54340-268-03, 54340-268-04
  • Packager: Henkel Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 25, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient

    Benzalkonium Chloride 0.10%

  • PURPOSE

    Purpose

    Antibacterial

  • INDICATIONS & USAGE

    Use

    • for washing to decrease bacteria on the skin.
  • WARNINGS

    Warnings

    For external use only

    When using this productavoid contact with the eyes. In case of eye contact, flush with water.

    Stop use and ask a doctor ifirritation and redness develops.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions

    • wet bar with water
    • lather vigorously and wash skin
    • rinse and dry thoroughly
  • INACTIVE INGREDIENT

    Inactive ingredientsSoap (Sodium Palmate* • Sodium Palm Kernelate* • Sodium Cocoate*) • Water • Glycerin • Stearic Acid* • Coconut Acid* • Palm Acid* • Palm Kernel Acid* • Fragrance • Sorbitol • Sodium Chloride • Tetrasodium Glutamate Diacetate •Titanium Dioxide • Yellow 5 • Alcohol • Yellow 8 • Red 4

    *Contains one or more of these ingredients

  • QUESTIONS

    Questions?1-800-258-DIAL (3425)

  • SPL UNCLASSIFIED SECTION

    Visit our website at www.dialsoap.com

    Made in Columbia

    Henkel®, TM, ©2023 Distributed by

    Henkel Corporation, Rocky Hill, CT 06067

  • PRINCIPAL DISPLAY PANEL

    DIAL® advanced clean™

    DEODORANT SOAP BAR

    ANTIBACTERIAL gold

    3-4 OZ SOAP BARS (113 g), TOTAL NET WT 12 OZ (339 g)

    DIAL GOLD ADV CLEAN 3 BAR

  • INGREDIENTS AND APPEARANCE
    DIAL ADVANCED CLEAN  ANTIBACTERIAL GOLD
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54340-268
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    FLUORESCEIN SODIUM (UNII: 93X55PE38X)  
    SODIUM PALMATE (UNII: S0A6004K3Z)  
    SODIUM COCOATE (UNII: R1TQH25F4I)  
    COCONUT ACID (UNII: 40U37V505D)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    SORBITOL (UNII: 506T60A25R)  
    TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)  
    PALM ACID (UNII: B6G0Y5Z616)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    PALM KERNEL ACID (UNII: 79P21R4317)  
    ALCOHOL (UNII: 3K9958V90M)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Product Characteristics
    Coloryellow (Gold) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54340-268-044 in 1 PACKET09/07/2022
    1113 g in 1 PACKAGE; Type 0: Not a Combination Product
    2NDC:54340-268-033 in 1 PACKET09/07/2022
    2113 g in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)09/07/2022
    Labeler - Henkel Corporation (080887708)
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