DIAL COMPLETE ANTIBACTERIAL LIQUID HAND GOLD- benzalkonium chloride solution

Dial Complete Antibacterial Liquid Hand by

Drug Labeling and Warnings

Dial Complete Antibacterial Liquid Hand by is a Otc medication manufactured, distributed, or labeled by MID-CONTINENT PACKAGING, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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 hands, wet as needed
• Lather vigorously for at least 15 seconds
• Wash skin, rinse thoroughly and dry

Inactive ingredients

Aqua (Water, Eau) Lauramidopropylamine Oxide Glycerin Cetrimonium Chloride Lauramine Oxide Sodium Chloride PEG-120 Methyl Glucose Dioleate Citric Acid Sodium Benzoate Myristamidopropylamine Oxide Zinc Sulfate Parfum (Fragrance) Dimethyl Lauramine Tetrasodium EDTA Alcohol Dimethyl Myristamine CI 19140 (Yellow 5) CI 14700 (Red 4)

Questions?

1-800-258-DIAL (3425)

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Distributed by
Henkel Corporation,
Rocky Hill, CT 06067

PRINCIPAL DISPLAY PANEL - 1.53 L Bottle Label

KILLS 99.9% OF BACTERIA*

NEW
LOOK!

Dial
COMPLETE®

LIQUID
antibacterial
Hand Soap

GOLD

52 FL OZ (1.62 QT) 1.53 L

2370135

INGREDIENTS AND APPEARANCE

DIAL COMPLETE ANTIBACTERIAL LIQUID HAND   GOLD
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69560-345
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzalkonium Chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	Benzalkonium Chloride	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Lauramidopropylamine Oxide (UNII: I6KX160QTV)
Lauramine Oxide (UNII: 4F6FC4MI8W)
Cetrimonium Chloride (UNII: UC9PE95IBP)
GLYCERIN (UNII: PDC6A3C0OX)
Sodium Chloride (UNII: 451W47IQ8X)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
Sodium Benzoate (UNII: OJ245FE5EU)
Edetate Sodium (UNII: MP1J8420LU)
Myristamidopropylamine Oxide (UNII: 3HSF539C9T)
Zinc Sulfate Heptahydrate (UNII: N57JI2K7WP)
Dimethyl Lauramine (UNII: 6V2OM30I1Z)
Alcohol (UNII: 3K9958V90M)
Dimethyl Myristamine (UNII: 5E4O85D8T2)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)

Product Characteristics
Color	ORANGE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69560-345-02	1530 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/05/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	05/05/2021

Labeler - MID-CONTINENT PACKAGING, INC. (798250239)