DIAL ANTIBACTERIAL AND SENSITIVE ALOE- dial antibacterial and sensitive deodorant bar soap hypoallergenic aloe scent soap

Dial Antibacterial and Sensitive Aloe by

Drug Labeling and Warnings

Dial Antibacterial and Sensitive Aloe 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* · Sorbitol · Fragrance · 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

Made in Colombia

Henkel®, TM, ©2024 Distributed by

Henkel Corporation, Rocky Hill, CT 06067

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DIAL ANTIBACTERIAL AND SENSITIVE ALOE 
dial antibacterial and sensitive deodorant bar soap hypoallergenic aloe scent soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54340-267
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)
SORBITOL (UNII: 506T60A25R)
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)
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)	0.058 g  in 100 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54340-267-03	450 in 1 CARTON	06/01/2025
1	NDC: 54340-267-02	16 in 1 CARTON
1	NDC: 54340-267-01	113 g in 1 CELLO PACK; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	06/01/2024

Labeler - Henkel Corporation (080887708)