Dial Antimicrobial

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

For handwashing to decrease bacteria on the skin

Warnings

For external use only.

Stop use and ask a doctor if

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 thouroughly and dry

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?

Call 1-800-258-DIAL (3425)

When using this product

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

DC81 DC82

DIAL ANTIMICROBIAL
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:57702-500
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	13 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:57702-500-08	221 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/17/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	12/17/2020

Labeler - Bocchi Laboratories (013579387)

Registrant - Henkel Corporation (081264055)

Name	Address	ID/FEI	Business Operations
Establishment
Bocchi Laboratories		013579387	manufacture(57702-500)