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]

SPL UNCLASSIFIED SECTION

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

Inactive ingredients Soap (Sodium Tallowate* Sodium Palmate* Sodium Cocoate* Sodium Palm Kernelate*) Aqua (Water, Eau) Glycerin Coconut Acid* Palm Acid* Palm Kernel Acid* Stearic Acid* Tallow Acid* Parfum (Fragrance) Sorbitol CI77891 (Titanium Dioxide) Sodium Chloride Tetrasodium Glutamate Diacetate Alcohol

*Contains one or more of these ingredients

QUESTIONS

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

SPL UNCLASSIFIED SECTION

Visit our website at www.dialsoap.com

Henkel®, TM, ©2021

Distributed by

Henkel Corporation,

Rocky Hill, CT 06067

Made in Columbia

PRINCIPAL DISPLAY PANEL

Dial COMPLETE®

spring water®

anti bacterial

CLEAN RINSING, NON-DRYING

DEODORANT SOAP BAR

SKIN SMART

moisturizing conditioners

gentle cleansers

free from parabens, phthalates, silicones

8-4 OZ SOAP BARS (113 g) TOTAL NET WT 32 OZ (904 g)

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: 54340-270-08	8 in 1 PACKAGE	03/08/2021
1		113 g in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 54340-270-12	12 in 1 PACKAGE	03/08/2021
2		113 g in 1 PACKET; Type 0: Not a Combination Product
3	NDC: 54340-270-13	113 g in 1 PACKET; Type 0: Not a Combination Product	01/31/2023
4	NDC: 54340-270-14	1356 g in 1 CELLO PACK; Type 0: Not a Combination Product	01/31/2023
5	NDC: 54340-270-15	904 g in 1 CELLO PACK; Type 0: Not a Combination Product	01/31/2023
6	NDC: 54340-270-16	339 g in 1 CELLO PACK; Type 0: Not a Combination Product	01/31/2023
7	NDC: 54340-270-17	181 g in 1 CELLO PACK; Type 0: Not a Combination Product	01/31/2023
8	NDC: 54340-270-18	678 g in 1 CELLO PACK; Type 0: Not a Combination Product	01/31/2023
9	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)