Label: DIAL ANTIBACTERIAL CALM AND SOOTHE- benzalkonium chloride soap

  • NDC Code(s): 54340-266-03, 54340-266-08, 54340-266-09, 54340-266-10
  • Packager: Henkel Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 14, 2023

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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 Palmate* • Sodium Palm Kernelate* • Sodium Cocoate*) • Water • Glycerin • Stearic Acid* • Coconut Acid* • Palm Acid* • Palm Kernel Acid* • Fragrance • Sorbitol • Sodium Chloride • Titanium Dioxide • Tetrasodium Glutamate Diacetate • Alcohol • Violet 2 • Red 33

    *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® calm & soothe™

    DEODORANT BAR SOAP

    ANTIBACTERIAL

    lavender & jasmine SCENT

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

    Dial LAVENDER JASMINE Soap

  • INGREDIENTS AND APPEARANCE
    DIAL ANTIBACTERIAL CALM AND SOOTHE 
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54340-266
    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
    ALCOHOL (UNII: 3K9958V90M) 0.01 g  in 100 g
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.3898 g  in 100 g
    SODIUM PALM KERNELATE (UNII: 6H91L1NXTW) 11.01 g  in 100 g
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) 0.3 g  in 100 g
    SORBITOL (UNII: 506T60A25R) 0.55 g  in 100 g
    GLYCERIN (UNII: PDC6A3C0OX) 8.1 g  in 100 g
    SODIUM PALMATE (UNII: S0A6004K3Z) 61.84 g  in 100 g
    STEARIC ACID (UNII: 4ELV7Z65AP) 2.435 g  in 100 g
    WATER (UNII: 059QF0KO0R) 13.95 g  in 100 g
    TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY) 0.058 g  in 100 g
    EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728) 0.0068 g  in 100 g
    D&C RED NO. 33 (UNII: 9DBA0SBB0L) 0.00092 g  in 100 g
    Product Characteristics
    Colorpurple (Lavender) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54340-266-033 in 1 PACKAGE09/07/2022
    1113 g in 1 PACKET; Type 0: Not a Combination Product
    2NDC:54340-266-088 in 1 PACKAGE09/07/2022
    2113 g in 1 PACKET; Type 0: Not a Combination Product
    3NDC:54340-266-09904 g in 1 CELLO PACK; Type 0: Not a Combination Product01/31/2023
    4NDC:54340-266-10339 g in 1 CELLO PACK; Type 0: Not a Combination Product01/31/2023
    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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