DIAL ANTIBACTERIAL CALM AND SOOTHE- benzalkonium chloride soap

Dial Antibacterial Calm and Soothe by

Drug Labeling and Warnings

Dial Antibacterial Calm and Soothe 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

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

Inactive ingredients Soap (Sodium Palmate* Sodium Palm Kernelate* Sodium Cocoate*) Water Glycerin Stearic Acid* Coconut Acid* Palm Acid* Palm Kernel Acid* Fragrance Sorbitol Sodium Chloride Titanium Dioxide Tetrasodium Glutamate Diacetate Alcohol Violet 2 Red 33

*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, ©2023 Distributed by

Henkel Corporation, Rocky Hill, CT 06067

PRINCIPAL DISPLAY PANEL

Dial® calm & soothe™

DEODORANT BAR SOAP

ANTIBACTERIAL

lavender & jasmine SCENT

3-4 OZ SOAP BARS (113 g), TOTAL NET WT 12 OZ (339 kg)

INGREDIENTS AND APPEARANCE

DIAL ANTIBACTERIAL CALM AND SOOTHE 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54340-266
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
ALCOHOL (UNII: 3K9958V90M)	0.01 g  in 100 g
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.3898 g  in 100 g
SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)	11.01 g  in 100 g
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)	0.3 g  in 100 g
SORBITOL (UNII: 506T60A25R)	0.55 g  in 100 g
GLYCERIN (UNII: PDC6A3C0OX)	8.1 g  in 100 g
SODIUM PALMATE (UNII: S0A6004K3Z)	61.84 g  in 100 g
STEARIC ACID (UNII: 4ELV7Z65AP)	2.435 g  in 100 g
WATER (UNII: 059QF0KO0R)	13.95 g  in 100 g
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)	0.058 g  in 100 g
EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)	0.0068 g  in 100 g
D&C RED NO. 33 (UNII: 9DBA0SBB0L)	0.00092 g  in 100 g

Product Characteristics
Color	purple (Lavender)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54340-266-03	3 in 1 PACKAGE	09/07/2022
1		113 g in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 54340-266-08	8 in 1 PACKAGE	09/07/2022
2		113 g in 1 PACKET; Type 0: Not a Combination Product
3	NDC: 54340-266-09	904 g in 1 CELLO PACK; Type 0: Not a Combination Product	01/31/2023
4	NDC: 54340-266-10	339 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)	09/07/2022

Labeler - Henkel Corporation (080887708)