Label: DIAL COMPLETE ANTIBACTERIAL FOAMING HAND WASH SPRING WATER- benzalkonium chloride solution

  • NDC Code(s): 69560-456-02, 69560-456-03
  • 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 December 16, 2021

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

  • 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 DRY hands
    • Lather vigorously for at least 15 seconds
    • Rinse and dry thoroughly
  • Inactive Ingredients

    Aqua (Water, Eau) • Glycerin • Lauramine Oxide • Cetrimonium Chloride • Cocamidopropyl Betaine • Citric Acid • Sodium Benzoate • Hydroxypropyl Methylcellulose • Parfum (Fragrance) • Zinc Sulfate • Sodium Chloride • Dimethyl Lauramine • Tetrasodium EDTA • Alcohol • Dimethyl Myristamine • CI 42090 (Blue 1) • CI17200 (Red 33)

  • SPL UNCLASSIFIED SECTION

    Distributed by Henkel
    Corporation, Rocky Hill, CT 06067

  • PRINCIPAL DISPLAY PANEL - 1.53 L Bottle Label

    KILLS 99.99% OF BACTERIA*

    #1 DR. RECOMMENDED#

    Dial
    COMPLETE®

    FOAMING
    antibacterial
    HAND WASH

    spring
    water®

    REFILL
    USE ONLY
    IN DIAL
    COMPLETE®
    FOAM PUMP

    SKIN
    SMART

    moisturizing conditioners
    gentle cleansers
    free from parabens,
    phthalates, silicones

    52 FL OZ (1.62 QT) 1.53 L REFILL

    2632116

    PRINCIPAL DISPLAY PANEL - 1.53 L Bottle Label
  • INGREDIENTS AND APPEARANCE
    DIAL COMPLETE ANTIBACTERIAL FOAMING HAND WASH   SPRING WATER
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69560-456
    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)  
    Lauramine Oxide (UNII: 4F6FC4MI8W)  
    Cetrimonium Chloride (UNII: UC9PE95IBP)  
    Glycerin (UNII: PDC6A3C0OX)  
    Cocamidopropyl Betaine (UNII: 5OCF3O11KX)  
    Anhydrous Citric Acid (UNII: XF417D3PSL)  
    Hypromellose, Unspecified (UNII: 3NXW29V3WO)  
    Sodium Benzoate (UNII: OJ245FE5EU)  
    Zinc Sulfate Heptahydrate (UNII: N57JI2K7WP)  
    Edetate Sodium (UNII: MP1J8420LU)  
    Dimethyl Lauramine (UNII: 6V2OM30I1Z)  
    Alcohol (UNII: 3K9958V90M)  
    Dimethyl Myristamine (UNII: 5E4O85D8T2)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    Product Characteristics
    ColorBLUEScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69560-456-021530 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/01/2021
    2NDC:69560-456-03946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart333E05/01/2021
    Labeler - MID-CONTINENT PACKAGING, INC. (798250239)