DIAL ANTIMICROBIAL- benzalkonium chloride liquid

Dial Antimicrobial by

Drug Labeling and Warnings

Dial Antimicrobial by is a Otc medication manufactured, distributed, or labeled by Bocchi Laboratories, Henkel Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

DIAL ANTIMICROBIAL 
benzalkonium chloride liquid

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

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

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 57702-500-08	221 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/17/2020

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

Labeler - Bocchi Laboratories (013579387)

Registrant - Henkel Corporation (081264055)

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