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, 54340-278-19
  • Packager: Henkel Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 10, 2023

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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

    Soap [Sodium Tallowate* • Sodium Palmate* • Sodium Cocoate* • Sodium Palm Kernelate*] • Aqua (Water, Eau) • Coconut Acid* • Palm Acid* • Palm Kernel Acid* • Tallow Acid* • Glycerin • PEG-6 Methyl Ether • Parfum (Fragrance) • Sodium Chloride • Pentasodium Pentetate • Tetrasodium Etidronate • CI 77891 (Titanium Dioxide)

    *Contains one or more of these ingredients

  • Questions?

    1-800-258-DIAL (3425)

  • PRINCIPAL DISPLAY PANEL

    54340-278-07 (12B 4oz - 2398448)

    54340-278-06 (10B 4oz - 2343044)

    54340-278-05 (8B 4oz - 2343032)

    54340-278-02 (3B 4oz - 2342060)

    54340-278-01 (2B 3.2oz - 2342054)

  • 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
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) 0.8 g  in 100 g
    SORBITOL (UNII: 506T60A25R) 0.5525 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:54340-278-10113 g in 1 CELLO PACK; Type 0: Not a Combination Product01/31/2023
    2NDC:54340-278-11339 g in 1 CELLO PACK; Type 0: Not a Combination Product01/31/2023
    3NDC:54340-278-09904 g in 1 CELLO PACK; Type 0: Not a Combination Product01/31/2023
    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 Product01/31/2023
    6NDC:54340-278-04678 g in 1 CELLO PACK; Type 0: Not a Combination Product01/31/2023
    7NDC:54340-278-19181 g in 1 CELLO PACK; Type 0: Not a Combination Product01/31/2020
    8NDC:54340-278-12452 g in 1 CELLO PACK; Type 0: Not a Combination Product01/31/2020
    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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