DIAL ANTIBACTERIAL BAR- dial manuka honey bar soap soap

Dial Antibacterial Bar by

Drug Labeling and Warnings

Dial Antibacterial Bar by is a Otc medication manufactured, distributed, or labeled by Henkel Corporation, VVF Kansas Services LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium Chloride 0.115%

Purpose

Antibacterial

Uses

• for washing to decrease the bacteria on the skin.

Warning

For external use only.

When using this product

• avoid contact with eyes. In case of eye contact, flush with water.

Stop using and ask doctor if

• irritation or redness develops.

Keep out of reach of children.

If swallowed, get medical help or contact Poison Control Center right away.

Directions

• wet bar with water
• lather vigorously and wash skin
• rinse and dry thoroughly

Inactive ingredients

Sodium Cocoyl Isethionate, Stearic Acid, Soap [Sodium Tallowate*,

Sodium Palmate*, Sodium Cocoate*, Sodium Palm Kernelate*],

Coconut Acid*, Aqua (Water, Eau), Sodium Isethionate,

Parfum (Fragrance), Glycerin, PEG-8, Guar Hydroxypropyltrimonium

Chloride, Palm Acid*, Palm Kernel Acid*, Tallow Acid*, Sodium Chloride,

Pentasodium Pentetate, Tetrasodium Etidronate, CI 77891 (Titanium Dioxide)

*contains one or more of these ingredients

QUESTIONS

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

SPL UNCLASSIFIED SECTION

Visit our web site at www.dialsoap.com

®, TM, © 2018 Distributed by

Henkel Corporation

Rocky Hill, CT 06067

SPL UNCLASSIFIED SECTION

Dial Complete

2 in 1 Moisturing

& antibacterial

Beauty Bar

Ultra-moisturizing formula from Dial ® gives you soft, smooth and radiant looking skin vs. ordinary soap.

Use on face and body

MANUKA HONEY

Also try our new moisturizing & antibacterial foaming hand wash!

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DIAL ANTIBACTERIAL BAR 
dial manuka honey bar soap soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54340-280
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.115 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)	53.7 g  in 100 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54340-280-01	49 g in 1 CARTON; Type 0: Not a Combination Product	09/25/2017
2	NDC: 54340-280-02	180 g in 1 CELLO PACK; Type 0: Not a Combination Product	09/25/2017
3	NDC: 54340-280-03	642 g in 1 CELLO PACK; Type 0: Not a Combination Product	09/25/2017
4	NDC: 54340-280-04	270 g in 1 CELLO PACK; Type 0: Not a Combination Product	09/25/2017
5	NDC: 54340-280-05	540 g in 1 CELLO PACK; Type 0: Not a Combination Product	07/02/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	09/25/2017

Labeler - Henkel Corporation (080887708)

Registrant - Henkel Corporation (080887708)

Establishment
Name	Address	ID/FEI	Business Operations
VVF Kansas Services LLC		833164242	manufacture(54340-280)