DAWNMIST UNSCENTED ROLL-ON ANTIPERSPIRANT DEODORANT- aluminum chlorohydrate solution

DawnMist Unscented Roll-On Antiperspirant Deodorant by

Drug Labeling and Warnings

DawnMist Unscented Roll-On Antiperspirant Deodorant by is a Otc medication manufactured, distributed, or labeled by Donovan Industries, Inc., Guangzhou Haishi Biological Technology Co., Ltd. . Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Aluminum Chlorohydrate 7.8%

PURPOSE

Purpose

Antiperspirant

INDICATIONS & USAGE

Use: Reduces underarm perspiration

WARNINGS

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

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

DOSAGE & ADMINISTRATION

Directions: Apply to underarms only.

INACTIVE INGREDIENT

Inactive Ingredients: Water, Mineral Oil, Polysorbate 60, Glycerin, Peg-100 Stearate, Sorbitan Monostearate, Ceteraryl Alcohol, Dimethicone, Magnesium Aluminum Silicate, Glyceryl Monostearate, Hydroxyethylcellulose, Sodium Benzoate, Methylparaben, Disodium EDTA, Propylparaben

SPL UNCLASSIFIED SECTION

Manufactured for:

Donovan Industries, Inc.

Tampa, Florida 33626-3061

800.334.4404

www.DawnMist.com

Made in China

PRINCIPAL DISPLAY PANEL

DawnMist

Fights Wetness and Odor

Unscented

Roll-On

Antiperspirant

Deodorant

2 FL. OZ 59ml

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DAWNMIST UNSCENTED ROLL-ON ANTIPERSPIRANT DEODORANT  
aluminum chlorohydrate solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55504-9002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	78 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
MINERAL OIL (UNII: T5L8T28FGP)
POLYSORBATE 60 (UNII: CAL22UVI4M)
GLYCERIN (UNII: PDC6A3C0OX)
POLYOXYL 100 STEARATE (UNII: YD01N1999R)
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
DIMETHICONE (UNII: 92RU3N3Y1O)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
METHYLPARABEN (UNII: A2I8C7HI9T)
EDETATE DISODIUM (UNII: 7FLD91C86K)
PROPYLPARABEN (UNII: Z8IX2SC1OH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55504-9002-1	59 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	10/01/2010

Labeler - Donovan Industries, Inc. (096662267)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Haishi Biological Technology Co., Ltd.		421262738	manufacture(55504-9002)