DAWNMIST ANTIPERSPIRANT DEODORANT- aluminum chlorohydrate liquid

DawnMist Antiperspirant Deodorant by

Drug Labeling and Warnings

DawnMist Antiperspirant Deodorant by is a Otc medication manufactured, distributed, or labeled by Dukal Corporation. 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.

Do not use

on broken skin.

Discontinue use if

■irritation and redness
develop ■ If condition persists for more than 72
hours consult a doctor.

Ask a doctor before use

if you have kidney disease.

Keep out of reach of children

■If swallowed, get medical help and contact Poison Control Center right away ■ Use only as directed

Directions

Apply to underarms only.

Inactive Ingredients

Water, Mineral Oil, Cetyl Alcohol, Ceteareth-24, Isopropyl Palmitate, Magnesium Aluminum Silicate, Methylparaben, Sodium Benzoate, Propylparaben

Package Label

INGREDIENTS AND APPEARANCE

DAWNMIST ANTIPERSPIRANT DEODORANT 
aluminum chlorohydrate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65517-1005
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
WATER (UNII: 059QF0KO0R)
MINERAL OIL (UNII: T5L8T28FGP)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65517-1005-1	59 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	01/10/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	01/10/2013

Labeler - Dukal Corporation (791014871)