DIAL ADVANCED CLEAN ANTIBACTERIAL GOLD- benzalkonium chloride soap

Dial advanced clean by

Drug Labeling and Warnings

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

Drug Details [pdf]

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Drug Facts

ACTIVE INGREDIENT

Active ingredient

Benzalkonium Chloride 0.1%

PURPOSE

Purpose

Antibacterial

INDICATIONS & USAGE

UseFor washing to decrease bacteria on the skin.

WARNINGS

Warnings

For external use only

When using this productavoid contact with eyes. In case of eye contact, flush with water.

Stop use and ask a doctor ifirritation and redness develops.

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

DOSAGE & ADMINISTRATION

Directions wet bar with water Lather vigorously and wash skin Rinse and dry thoroughly

INACTIVE INGREDIENT

Inactive ingredientsSoap [Sodium Palmate* Sodium Palm Kernelate* Sodium Cocoate*] Water Glycerin Stearic Acid* Coconut Acid* Palm Acid* Palm Kernel 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

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

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Visit our website at www.dialsoap.com

Made in Columbia

Henkel®, TM, ©2024 Distributed by

Henkel Corporation, Rocky Hill, CT 06067

PRINCIPAL DISPLAY PANEL

ELIMINATES 99% OF BACTERIA**

Dial ®advanced clean™

DEODORANT BAR SOAP

ANTIBACTERIAL

gold

NET WT 4 OZ (113 g)

INGREDIENTS AND APPEARANCE

DIAL ADVANCED CLEAN  ANTIBACTERIAL GOLD
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54340-262
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: 54340-262-12	12 in 1 PACKAGE	01/02/2023
1		113 g in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 54340-262-08	8 in 1 PACKAGE	01/02/2023
2		113 g in 1 PACKET; Type 0: Not a Combination Product
3	NDC: 54340-262-01	113 g in 1 PACKET; Type 0: Not a Combination Product	01/02/2023
4	NDC: 54340-262-03	3 in 1 PACKAGE	01/02/2023
4		113 g in 1 PACKET; Type 0: Not a Combination Product
5	NDC: 54340-262-04	4 in 1 PACKAGE	01/02/2023
5		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)	01/02/2023

Labeler - Henkel Corporation (080887708)