DIAL COMPLETE ANTIBACTERIAL BAR SPRING WATER- benzalkonium chloride soap

Dial Complete Antibacterial Bar by

Drug Labeling and Warnings

Dial Complete Antibacterial Bar 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 0.10%

PURPOSE

Purpose

Antibacterial

INDICATIONS & USAGE

Use

For washing to decrease bacteria on the skin.

WARNINGS

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

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

Soap[Sodium Palmate* · Sodium Palm Kernelate* · Sodium Cocoate*] · Water · Glycerin · Stearic Acid* · Coconut Acid* · Palm Acid* · Palm Kernel Acid* · Fragrance · Titanium Dioxide · Sorbitol · Sodium Chloride · Tetrasodium Glutamate Diacetate · Alcohol
*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

Henkel®, TM, ©2023

Distributed by

Henkel Corporation,

Rocky Hill, CT 06067

Made in Columbia

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DIAL COMPLETE ANTIBACTERIAL BAR  SPRING WATER
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54340-270
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
WATER (UNII: 059QF0KO0R)	13.95 g  in 100 g
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.39 g  in 100 g
GLYCERIN (UNII: PDC6A3C0OX)	8.05 g  in 100 g
SODIUM PALMATE (UNII: S0A6004K3Z)	61.81 g  in 100 g
STEARIC ACID (UNII: 4ELV7Z65AP)	2.434 g  in 100 g
ALCOHOL (UNII: 3K9958V90M)	0.01 g  in 100 g
SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)	11 g  in 100 g
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)	0.8 g  in 100 g
SORBITOL (UNII: 506T60A25R)	0.5525 g  in 100 g
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)	0.058 g  in 100 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54340-270-13	113 g in 1 PACKET; Type 0: Not a Combination Product	01/31/2023
2	NDC: 54340-270-14	1356 g in 1 CELLO PACK; Type 0: Not a Combination Product	01/31/2023
3	NDC: 54340-270-15	904 g in 1 CELLO PACK; Type 0: Not a Combination Product	01/31/2023
4	NDC: 54340-270-16	339 g in 1 CELLO PACK; Type 0: Not a Combination Product	01/31/2023
5	NDC: 54340-270-17	181 g in 1 CELLO PACK; Type 0: Not a Combination Product	01/31/2023	01/01/2024
6	NDC: 54340-270-18	678 g in 1 CELLO PACK; Type 0: Not a Combination Product	01/31/2023	01/01/2024
7	NDC: 54340-270-19	452 g in 1 CELLO PACK; Type 0: Not a Combination Product	01/31/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	03/08/2021

Labeler - Henkel Corporation (080887708)