Label: DIAL COMPLETE ANTIBACTERIAL LIQUID HAND GOLD- benzalkonium chloride solution

  • NDC Code(s): 69560-345-02
  • Packager: MID-CONTINENT PACKAGING, INC.
  • 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 April 26, 2021

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antibacterial

  • Uses

    • For handwashing 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 irritation or redness develops.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Pump into hands, wet as needed
    • Lather vigorously for at least 15 seconds
    • Wash skin, rinse thoroughly and dry
  • Inactive ingredients

    Aqua (Water, Eau) • Lauramidopropylamine Oxide • Glycerin • Cetrimonium Chloride • Lauramine Oxide • Sodium Chloride • PEG-120 Methyl Glucose Dioleate • Citric Acid • Sodium Benzoate • Myristamidopropylamine Oxide • Zinc Sulfate • Parfum (Fragrance) • Dimethyl Lauramine • Tetrasodium EDTA • Alcohol • Dimethyl Myristamine • CI 19140 (Yellow 5) • CI 14700 (Red 4)

  • Questions?

    1-800-258-DIAL (3425)

  • SPL UNCLASSIFIED SECTION

    Distributed by
    Henkel Corporation,
    Rocky Hill, CT 06067

  • PRINCIPAL DISPLAY PANEL - 1.53 L Bottle Label

    KILLS 99.9% OF BACTERIA*

    NEW
    LOOK!

    Dial
    COMPLETE®

    LIQUID
    antibacterial
    Hand Soap

    GOLD

    52 FL OZ (1.62 QT) 1.53 L

    2370135

    PRINCIPAL DISPLAY PANEL - 1.53 L Bottle Label
  • INGREDIENTS AND APPEARANCE
    DIAL COMPLETE ANTIBACTERIAL LIQUID HAND   GOLD
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69560-345
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Benzalkonium Chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) Benzalkonium Chloride1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Lauramidopropylamine Oxide (UNII: I6KX160QTV)  
    Lauramine Oxide (UNII: 4F6FC4MI8W)  
    Cetrimonium Chloride (UNII: UC9PE95IBP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Sodium Chloride (UNII: 451W47IQ8X)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Sodium Benzoate (UNII: OJ245FE5EU)  
    Edetate Sodium (UNII: MP1J8420LU)  
    Myristamidopropylamine Oxide (UNII: 3HSF539C9T)  
    Zinc Sulfate Heptahydrate (UNII: N57JI2K7WP)  
    Dimethyl Lauramine (UNII: 6V2OM30I1Z)  
    Alcohol (UNII: 3K9958V90M)  
    Dimethyl Myristamine (UNII: 5E4O85D8T2)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    Product Characteristics
    ColorORANGEScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69560-345-021530 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/05/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart333E05/05/2021
    Labeler - MID-CONTINENT PACKAGING, INC. (798250239)
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