Label: DIAL ANTIBACTERIAL BAR- dial white antibacterial bar soap soap

  • NDC Code(s): 54340-278-04, 54340-278-06, 54340-278-08, 54340-278-09, view more
    54340-278-10, 54340-278-11, 54340-278-12, 54340-278-13, 54340-278-14, 54340-278-15, 54340-278-16, 54340-278-19
  • Packager: Henkel Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 13, 2025

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  • Active Ingredient

    Benzalkonium Chloride 0.10%

  • Purpose

    Antibacterial

  • Uses

    • for washing to decrease the bacteria on the skin
  • Warnings

    For external use only

    When using this product

    • avoid contact with eyes. In case of eye contact, flush with water.

    Stop using and ask doctor if

    • irritation or redness develops

    Keep out of reach of children.

    If swallowed, get medical help or contact Poison Control Center right away.

  • Directions

    • wet bar with water
    • lather vigorously and wash skin
    • rinse and dry thoroughly
  • Inactive ingredients

    Sodium Palmate
    Water
    Sodium Palm Kernelate

    Sodium Cocoate

    Coconut Acid

    Palm Kernel acid

    Palm Acid

    Stearic Acid
    Glycerin
    Stearic Acid
    CI 77891 (Titanium Dioxide)
    Fragrance
    Sorbitol
    Sodium Chloride
    Tetrasodium Glutamate Diacetate
    Alcohol

    CONTAINS ONE OR MORE OF THESE INGREDIENTS

    Ingredients

    Ingredients-2

  • Questions?

    1-800-258-DIAL (3425)

  • PRINCIPAL DISPLAY PANEL

    Full art

    FOP 8 bars

    DFB 8 bars

  • INGREDIENTS AND APPEARANCE
    DIAL ANTIBACTERIAL BAR 
    dial white antibacterial bar soap soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54340-278
    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
    SORBITOL (UNII: 506T60A25R) 0.5525 g  in 100 g
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) 0.8 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
    GLYCERIN (UNII: PDC6A3C0OX) 8.1 g  in 100 g
    ALCOHOL (UNII: 3K9958V90M) 0.01 g  in 100 g
    SODIUM PALMATE (UNII: S0A6004K3Z) 61.87 g  in 100 g
    TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY) 0.058 g  in 100 g
    STEARIC ACID (UNII: 4ELV7Z65AP) 2.4365 g  in 100 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54340-278-1336 in 1 CARTON02/01/2023
    1NDC:54340-278-10113 g in 1 CELLO PACK; Type 0: Not a Combination Product
    2NDC:54340-278-1412 in 1 CARTON02/01/2023
    2NDC:54340-278-11339 g in 1 CELLO PACK; Type 0: Not a Combination Product
    3NDC:54340-278-154 in 1 CARTON02/01/2023
    3NDC:54340-278-09904 g in 1 CELLO PACK; Type 0: Not a Combination Product
    4NDC:54340-278-061130 g in 1 CELLO PACK; Type 0: Not a Combination Product07/01/201702/07/2023
    5NDC:54340-278-081356 g in 1 CELLO PACK; Type 0: Not a Combination Product02/01/2023
    6NDC:54340-278-04678 g in 1 CELLO PACK; Type 0: Not a Combination Product01/31/202312/06/2024
    7NDC:54340-278-19181 g in 1 CELLO PACK; Type 0: Not a Combination Product01/31/202001/01/2023
    8NDC:54340-278-168 in 1 CARTON02/01/2023
    8NDC:54340-278-12452 g in 1 CELLO PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/01/2017
    Labeler - Henkel Corporation (080887708)
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