Dial Complete Antibacterial Soap Gold

Dial Complete by

Drug Labeling and Warnings

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

Drug Details [pdf]

DIAL COMPLETE GOLD ANTIBACTERIAL- benzalkonium chloride soap 
Henkel Corporation

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Dial Complete Antibacterial Soap Gold

Drug Facts

Active ingredient

Benzalkonium Chloride 0.1%

Purpose

Antibacterial

Use For washing to decrease bacteria on the skin.

Warnings

For external use only

When using this product avoid contact with the eyes. In case of eye contact, flush with water.

Stop use and ask a doctor if irritation and redness develops.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Wet bar with water. Lather vigorously and wash skin. Rinse and dry thoroughly.

Inactive ingredients Soap (Sodium Tallowate* Sodium Palmate* Sodium Cocoate* Sodium Palm Kernelate*) Water Glycerin Coconut Acid* Palm Acid* Palm Kernel Acid* Stearic Acid* Fragrance Sorbitol Sodium Chloride Tetrasodium Glutamate Diacetate Titanium Dioxide Yellow 5 Alcohol Yellow 8 Red 4

*Contains one or more of these ingredients

Questions? 1-800-258-DIAL (3425)

Visit our website at www.dialsoap.com

Henkel®, TM, ©2021 Distributed by

Henkel Corporation, Rocky Hill, CT 06067

Made in Columbia

Dial COMPLETE®

12 BARS

gold antibacterial

ELIMINATES 99% OF BACTERIA**

CLEAN RINSING, NON-DRYING

DEODORANT BAR SOAP

moisturizing conditioners

gentle cleansers

free from parabens, phthalates, silicones

12-4 OZ SOAP BARS (113 g) EACH, TOTAL NET WT 48 OZ (1.35 kg)

DIAL COMPLETE  GOLD ANTIBACTERIAL
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54340-269
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
SODIUM PALMATE (UNII: S0A6004K3Z)
SODIUM COCOATE (UNII: R1TQH25F4I)
COCONUT ACID (UNII: 40U37V505D)
STEARIC ACID (UNII: 4ELV7Z65AP)
SORBITOL (UNII: 506T60A25R)
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
PALM ACID (UNII: B6G0Y5Z616)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
PALM KERNEL ACID (UNII: 79P21R4317)
ALCOHOL (UNII: 3K9958V90M)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)
FLUORESCEIN SODIUM (UNII: 93X55PE38X)

Product Characteristics
Color	yellow (Gold)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54340-269-12	12 in 1 PACKAGE	03/10/2022	12/28/2024
1		113 g in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 54340-269-08	8 in 1 PACKAGE	03/10/2022	12/28/2024
2		113 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	03/10/2022	12/28/2024

Labeler - Henkel Corporation (080887708)

Revised: 1/2024

Document Id: 0dfa4948-6ba4-bc88-e063-6294a90a87b6

34390-5

Set id: d9e2dfe9-2cf0-58b4-e053-2a95a90aa9a2

Version: 2

Effective Time: 20240101