Label: DIAL COMPLETE WHITE ANTIBACTERIAL- benzalkonium chloride soap

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

Drug Label Information

Updated January 1, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient

    Benzalkonium Chloride 0.1%

  • PURPOSE

    Purpose

    Antibacterial

  • INDICATIONS & USAGE

    Use For washing to decrease bacteria on the skin

  • WARNINGS

    Warnings

    For external use only

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

    Stop use and ask a doctor if irritation 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 ingredients Soap (Sodium Tallowate* • Sodium Palmate* • Sodium Cocoate* • Sodium Palm Kernelate*) • Water • Glycerin • Coconut Acid* • Palm Acid* • Palm Kernel Acid* • Stearic Acid* • Tallow Acid* • Sorbitol • Fragrance • Titanium Dioxide • Sodium Chloride • Tetrasodium Glutamate Diacetate • Alcohol

    *Contains one or more of these ingredients

  • QUESTIONS

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

  • SPL UNCLASSIFIED SECTION

    Visit our website at www.dialsoap.com

    Henkel®, TM, ©2021 Distributed by

    Henkel Corporation, Rocky Hill, CT 06067

    Made in Columbia

  • PRINCIPAL DISPLAY PANEL

    Dial COMPLETE®

    12 BARS

    white antibacterial

    ELIMINATES 99% OF BACTERIA**

    CLEAN RINSING, NON-DRYING

    DEODORANT BAR SOAP

    moisturizing conditioners

    gentle cleansers

    free from parabens, phthalates, silicones

    12-4 OZ SOAP BARS (113 g) EACH, TOTAL NET WT 48 OZ (1.35 kg)

    label

  • INGREDIENTS AND APPEARANCE
    DIAL COMPLETE  WHITE ANTIBACTERIAL
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54340-265
    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
    SODIUM PALMATE (UNII: S0A6004K3Z)  
    SODIUM COCOATE (UNII: R1TQH25F4I)  
    COCONUT ACID (UNII: 40U37V505D)  
    TALLOW ACID, BEEF (UNII: 5U9XZ261ER)  
    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)  
    SODIUM TALLOWATE, BEEF (UNII: 07RIK6QMEW)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54340-265-1212 in 1 PACKAGE07/22/202112/28/2024
    1113 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)07/22/202112/28/2024
    Labeler - Henkel Corporation (080887708)
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