Label: DIAL ANTIBACTERIAL AND SENSITIVE ALOE- dial antibacterial and sensitive deodorant bar soap hypoallergenic aloe scent soap

  • NDC Code(s): 54340-267-01, 54340-267-02
  • Packager: Henkel Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 25, 2024

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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* · Sorbitol · Fragrance · Sodium Chloride · Tetrasodium Glutamate Diacetate · Alcohol *Contains one or more of these ingredients

    Ingredients

    FOP

  • QUESTIONS

    Questions? 1-800-258-DIAL (3425)

  • SPL UNCLASSIFIED SECTION

    Visit our website at www.dialsoap.com

    Made in Colombia

    Henkel®, TM, ©2024 Distributed by

    Henkel Corporation, Rocky Hill, CT 06067

  • PRINCIPAL DISPLAY PANEL

    Aloe FOP

    DFB

  • INGREDIENTS AND APPEARANCE
    DIAL ANTIBACTERIAL AND SENSITIVE ALOE 
    dial antibacterial and sensitive deodorant bar soap hypoallergenic aloe scent soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54340-267
    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)  
    SORBITOL (UNII: 506T60A25R)  
    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)  
    TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY) 0.058 g  in 100 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54340-267-0216 in 1 CARTON06/01/2024
    1NDC:54340-267-01113 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)06/01/2024
    Labeler - Henkel Corporation (080887708)
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