Label: DIAL ANTIBACTERIAL BAR- dial vitamins antibacterial soap soap

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated December 29, 2022

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  • Active Ingredient

    Benzalkonium Chloride 0.10%

  • Purpose

    Antibacterial

  • Uses

    For washing to decrease 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 use and ask a doctor if

    • irration and 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),

    Glycerin, Coconut Acid*, Palm Acid*,

    Palm Kernel Acid*, Tallow Acid*,

    Parfum (Fragrance), PEG-8, Tocopheryl

    Acetate, Panthenol, Retinyl Palmitate,

    Sodium Chloride, Pentasodium

    Pentetate, Tetrasodium Etidronate,

    CI 19140 (Yellow 5), CI 14700 (Red 4)

    *contains one or more of these ingredients

  • QUESTIONS

    Questions? 1-800-253-DIAL

  • SPL UNCLASSIFIED SECTION

    HENKEL

    ®, TM, © 2017 DISTRIBUTED BY

    THE DIAL CORPORATION,

    SCOTTSDALE, AZ 85255 / AFTER 1/1/2018

    HENKEL CORPORATION, ROCKY HILL, CT 06067

    MANUFACTURED IN USA

    www. dialprofessional.com

    CM-1-00072-05/2238822

    U.S. Patent: 6,706,675

    UPC: 010923000728

  • PRINCIPAL DISPLAY PANEL

    Dial Vitamins Overwrap

  • INGREDIENTS AND APPEARANCE
    DIAL ANTIBACTERIAL BAR 
    dial vitamins antibacterial soap soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54340-282
    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 TALLOWATE, BEEF (UNII: 07RIK6QMEW) 48.5 g  in 100 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54340-282-01113 g in 1 CELLO PACK; Type 0: Not a Combination Product10/02/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E10/02/201712/31/2025
    Labeler - Henkel Corporation (080887708)
    Registrant - Henkel Corporation (080887708)
    Establishment
    NameAddressID/FEIBusiness Operations
    VVF Kansas Services LLC833164242manufacture(54340-282)
    Establishment
    NameAddressID/FEIBusiness Operations
    VVF Illinois Services LLC024177178manufacture(54340-282)
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