Label: DIAL ADVANCED CLEAN ANTIBACTERIAL GOLD- benzalkonium chloride soap

  • NDC Code(s): 54340-262-01, 54340-262-03, 54340-262-04, 54340-262-08, view more
    54340-262-12
  • Packager: Henkel Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 11, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient

    Benzalkonium Chloride 0.1%

  • PURPOSE

    Purpose

    Antibacterial

  • INDICATIONS & USAGE

    UseFor washing to decrease bacteria on the skin.

  • WARNINGS

    Warnings

    For external use only

    When using this productavoid contact with 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. 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, ©2024 Distributed by

    Henkel Corporation, Rocky Hill, CT 06067

  • PRINCIPAL DISPLAY PANEL

    ELIMINATES 99% OF BACTERIA**

    Dial ®advanced clean™

    DEODORANT BAR SOAP

    ANTIBACTERIAL

    gold

    NET WT 4 OZ (113 g)

    1 bar label

    12 count label

  • INGREDIENTS AND APPEARANCE
    DIAL ADVANCED CLEAN  ANTIBACTERIAL GOLD
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54340-262
    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)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    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)  
    FLUORESCEIN SODIUM (UNII: 93X55PE38X)  
    Product Characteristics
    Coloryellow (Gold) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54340-262-1212 in 1 PACKAGE01/02/2023
    1113 g in 1 PACKET; Type 0: Not a Combination Product
    2NDC:54340-262-088 in 1 PACKAGE01/02/2023
    2113 g in 1 PACKET; Type 0: Not a Combination Product
    3NDC:54340-262-01113 g in 1 PACKET; Type 0: Not a Combination Product01/02/2023
    4NDC:54340-262-033 in 1 PACKAGE01/02/2023
    4113 g in 1 PACKET; Type 0: Not a Combination Product
    5NDC:54340-262-044 in 1 PACKAGE01/02/2023
    5113 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/02/2023
    Labeler - Henkel Corporation (080887708)
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