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

  • NDC Code(s): 54340-272-21, 54340-272-22, 54340-272-28, 54340-272-35, view more
    54340-272-36, 54340-272-37, 54340-272-38, 54340-272-39
  • Packager: Henkel Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 14, 2023

If you are a consumer or patient please visit this version.

  • Active ingredient

    Benzalkonium Chloride 0.10%

  • Purpose

    Antibacterial

  • Uses

    • for washing to decrease the bacterial 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 a 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 19140 (Yellow 5) • CI 45350 (Yellow 8) • CI 14700 (Red 4)
    *Contains one or more of these ingredients

  • PRINCIPAL DISPLAY PANEL

    54340-272-20 (1B 3.5oz - 2405260)

    54340-272-21 (2B 3.2oz - 2342052)

    54340-272-22 (3B 4oz - 2342061)

    54340-272-23 (6B 3.2oz - 2342969)

    54340-272-24 (6B 4oz - 2342980)

    54340-272-25 (8B 4oz - 2343029)

    54340-272-26 (10B 4oz - 2184688)

    54340-272-27 (12B 4oz - 2343049)

    54340-272-28 (1B 2.25oz - 2342045)

  • INGREDIENTS AND APPEARANCE
    DIAL ANTIBACTERIAL BAR 
    dial gold antibacterial bar soap soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54340-272
    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
    GLYCERIN (UNII: PDC6A3C0OX) 8.1 g  in 100 g
    WATER (UNII: 059QF0KO0R) 14.086 g  in 100 g
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.393 g  in 100 g
    BASIC YELLOW 87 (UNII: 224I63D8K4) 0.00216 g  in 100 g
    BASIC RED 46 (UNII: 58KJM7T349) 0.00099 g  in 100 g
    SODIUM PALM KERNELATE (UNII: 6H91L1NXTW) 11.07 g  in 100 g
    SORBITOL (UNII: 506T60A25R) 0.652 g  in 100 g
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M) 0.0182 g  in 100 g
    TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY) 0.0588 g  in 100 g
    STEARIC ACID (UNII: 4ELV7Z65AP) 2.45 g  in 100 g
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) 0.035 g  in 100 g
    ALCOHOL (UNII: 3K9958V90M) 0.01 g  in 100 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54340-272-22181 g in 1 CELLO PACK; Type 0: Not a Combination Product01/31/2023
    2NDC:54340-272-39452 g in 1 CELLO PACK; Type 0: Not a Combination Product01/31/2023
    3NDC:54340-272-38339 g in 1 CELLO PACK; Type 0: Not a Combination Product01/31/2023
    4NDC:54340-272-36904 g in 1 CELLO PACK; Type 0: Not a Combination Product01/31/2023
    5NDC:54340-272-351356 g in 1 CELLO PACK; Type 0: Not a Combination Product01/31/2023
    6NDC:54340-272-2863 g in 1 CARTON; Type 0: Not a Combination Product03/01/2023
    7NDC:54340-272-21678 g in 1 CELLO PACK; Type 0: Not a Combination Product01/31/2023
    8NDC:54340-272-37113 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)03/01/2017
    Labeler - Henkel Corporation (080887708)