Label: DIAL ANTIMICROBIAL- benzalkonium chloride liquid

  • 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 January 11, 2021

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

View All Sections
  • ACTIVE INGREDIENT

    Active Ingredient

    Benzalkonium Chloride 0.13%

  • PURPOSE

    Purpose

    Antibacterial

  • INDICATIONS & USAGE

    Uses

    • For handwashing to decrease bacteria on the skin
  • WARNINGS

    Warnings

    For external use only.

  • STOP USE

    Stop use and ask a doctor if

    • if irritation or 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

    • Pump into hands, wet as needed
    • Lather vigorously for at least 15 seconds
    • Wash skin, rinse thouroughly and dry
  • INACTIVE INGREDIENT

    Aqua (Water, Eau), Lauramidopropylamine Oxide, Glycerin, Lauramine Oxide, Cetrimonium Chloride, Sodium Chloride, PEG-120 Methyl Glucose Dioleate, Citric Acid, Sodium Benzoate, Myristamidopropylamine Oxide, Parfum (Fragrance), Zinc Sulfate, Dimethyl Lauramine, Tetrasodium EDTA, Alcohol, Camellia Sinensis Leaf Extract, Dimethyl Myristamine, CI 42090 (Blue 1), CI 17200 (Red 33)

  • QUESTIONS

    Questions?

    Call 1-800-258-DIAL (3425)

  • WHEN USING

    When using this product

    Avoid contact with eyes, in case of eye contact, flush with water

  • PRINCIPAL DISPLAY PANEL

    DC81DC82

  • INGREDIENTS AND APPEARANCE
    DIAL ANTIMICROBIAL 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57702-500
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE13 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    DIMETHYL LAURAMINE (UNII: 6V2OM30I1Z)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    WATER (UNII: 059QF0KO0R)  
    DIMETHYL MYRISTAMINE (UNII: 5E4O85D8T2)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)  
    ALCOHOL (UNII: 3K9958V90M)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    CHAMOMILE (UNII: FGL3685T2X)  
    ZINC SULFATE (UNII: 89DS0H96TB)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57702-500-08221 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/17/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A12/17/2020
    Labeler - Bocchi Laboratories (013579387)
    Registrant - Henkel Corporation (081264055)
    Establishment
    NameAddressID/FEIBusiness Operations
    Bocchi Laboratories013579387manufacture(57702-500)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!