DAWNMIST ANTIPERSPIRANT- aluminum chlorohydrate liquid

DawnMist Antiperspirant by

Drug Labeling and Warnings

DawnMist Antiperspirant by is a Otc medication manufactured, distributed, or labeled by Dukal LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Aluminum Chlorohydrate 4.5%

Purpose

Antiperspirant

Use

Reduces underarm perspiration

Warnings

For external use only.

Flammable, keep away from fire or flame.

Do not use

Do not use on broken skin

Stop use

Stop use if rash or irritation occurs.

Ask a doctor before use

Ask a doctor before use if you have kidney disease.

Keep out of reach of children

Keep out of reach of children. If accidently swallowed, get medical help or contact Poison Control Center right away.

Directions

Apply to underarms only.

Inactive ingredients

Alcohol, Fragrance, PEG-40 Hydrogenated Castor Oil, Water

PRINCIPAL DISPLAY PANEL

DawnMist

Antiperspirant

Spray

Fresh Scent

NDC: 65517-2030-1

Dukal

2FL.OZ. (59ml)

PRINCIPAL DISPLAY PANEL

NDC: 65517-2030-2

DawnMist

Personal Care

Antiperspirant

Spray

Fresh Scent

4FL.OZ. (118ml)

INGREDIENTS AND APPEARANCE

DAWNMIST ANTIPERSPIRANT 
aluminum chlorohydrate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65517-2030
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	45 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
WATER (UNII: 059QF0KO0R)
ALCOHOL 95% (UNII: 7528N5H79B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65517-2030-1	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	12/05/2024
2	NDC: 65517-2030-2	118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	12/05/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	12/05/2024

Labeler - Dukal LLC (791014871)