DIAL REFRESH AND RENEW ANTIBACTERIAL WHITE- benzalkonium chloride soap

Dial refresh and renew by

Drug Labeling and Warnings

Dial refresh and renew 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. 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* Titanium Dioxide Fragrance Sorbitol 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 ® refresh & renew™

Antibacterial white

DEODORANT BAR SOAP

ELIMINATES 99% OF BACTERIA**

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

INGREDIENTS AND APPEARANCE

DIAL REFRESH AND RENEW  ANTIBACTERIAL WHITE
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54340-260
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
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)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54340-260-12	12 in 1 PACKAGE	01/02/2023
1		113 g in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 54340-260-03	3 in 1 PACKAGE	01/02/2023
2		113 g in 1 PACKET; Type 0: Not a Combination Product
3	NDC: 54340-260-01	113 g in 1 PACKET; Type 0: Not a Combination Product	01/02/2023
4	NDC: 54340-260-04	4 in 1 PACKAGE	01/02/2023
4		113 g in 1 PACKET; Type 0: Not a Combination Product
5	NDC: 54340-260-08	8 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 not final	part333E	01/02/2023

Labeler - Henkel Corporation (080887708)