DIAL COMPLETE ANTIBACTERIAL FOAMING HAND WASH SPRING WATER- benzalkonium chloride solution

Dial Complete Antibacterial Foaming Hand Wash by

Drug Labeling and Warnings

Dial Complete Antibacterial Foaming Hand Wash 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 DRY hands
• Lather vigorously for at least 15 seconds
• Rinse and dry thoroughly

Inactive Ingredients

Aqua (Water, Eau) Glycerin Lauramine Oxide Cetrimonium Chloride Cocamidopropyl Betaine Citric Acid Sodium Benzoate Hydroxypropyl Methylcellulose Parfum (Fragrance) Zinc Sulfate Sodium Chloride Dimethyl Lauramine Tetrasodium EDTA Alcohol Dimethyl Myristamine CI 42090 (Blue 1) CI17200 (Red 33)

SPL UNCLASSIFIED SECTION

Distributed by Henkel
Corporation, Rocky Hill, CT 06067

PRINCIPAL DISPLAY PANEL - 1.53 L Bottle Label

KILLS 99.99% OF BACTERIA*

#1 DR. RECOMMENDED#

Dial
COMPLETE®

FOAMING
antibacterial
HAND WASH

spring
water®

REFILL
USE ONLY
IN DIAL
COMPLETE®
FOAM PUMP

SKIN
SMART

moisturizing conditioners
gentle cleansers
free from parabens,
phthalates, silicones

52 FL OZ (1.62 QT) 1.53 L REFILL

2632116

INGREDIENTS AND APPEARANCE

DIAL COMPLETE ANTIBACTERIAL FOAMING HAND WASH   SPRING WATER
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69560-456
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)
Lauramine Oxide (UNII: 4F6FC4MI8W)
Cetrimonium Chloride (UNII: UC9PE95IBP)
Glycerin (UNII: PDC6A3C0OX)
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)
Anhydrous Citric Acid (UNII: XF417D3PSL)
Hypromellose, Unspecified (UNII: 3NXW29V3WO)
Sodium Benzoate (UNII: OJ245FE5EU)
Zinc Sulfate Heptahydrate (UNII: N57JI2K7WP)
Edetate Sodium (UNII: MP1J8420LU)
Dimethyl Lauramine (UNII: 6V2OM30I1Z)
Alcohol (UNII: 3K9958V90M)
Dimethyl Myristamine (UNII: 5E4O85D8T2)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Product Characteristics
Color	BLUE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69560-456-02	1530 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/01/2021
2	NDC: 69560-456-03	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	05/01/2021

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