DIAL ANTIMICROBIAL- benzalkonium chloride liquid 
Bocchi Laboratories

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.

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Dial Antimicrobial

Active Ingredient



Benzalkonium Chloride 0.13%

Purpose



Antibacterial

Uses

Warnings

For external use only.

Stop use and ask a doctor if

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control center right away.

Directions

Aqua (Water, Eau), Glycerin, Lauramine Oxide, Cetrimonium Chloride, Cocamidopropyl Betaine, Sodium Benzoate, Hydroxypropyl Methylcellulose, Parfum (Fragrance), Zinc Sulfate, Sodium Chloride, Dimethyl Lauramine, Tetrasodium EDTA, Alcohol, Dimethyl Myristamine, CI 42090 (Blue 1), CI 17200 (Red 33).

When using this product

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

DFHW

DIAL ANTIMICROBIAL 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57702-501
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)  
GLYCERIN (UNII: PDC6A3C0OX)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
WATER (UNII: 059QF0KO0R)  
DIMETHYL MYRISTAMINE (UNII: 5E4O85D8T2)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
ALCOHOL (UNII: 3K9958V90M)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
ZINC SULFATE (UNII: 89DS0H96TB)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
EDETATE SODIUM (UNII: MP1J8420LU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:57702-501-08221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/07/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/07/2021
Labeler - Bocchi Laboratories (013579387)
Registrant - Henkel Corporation (081264055)
Establishment
NameAddressID/FEIBusiness Operations
Bocchi Laboratories013579387manufacture(57702-501)

Revised: 5/2021
Document Id: c2192983-842e-510e-e053-2a95a90a2429
Set id: c2192969-7a24-16c6-e053-2a95a90ad979
Version: 1
Effective Time: 20210511
 
Bocchi Laboratories