DAWNMIST ANTIPERSPIRANT DEODORANT- aluminum chlorohydrate lotion

DawnMist Antiperspirant Deodorant by

Drug Labeling and Warnings

DawnMist Antiperspirant Deodorant by is a Otc medication manufactured, distributed, or labeled by Dukal Corporation, KEN PRIMA COSMECEUTICALS SDN. BHD.. 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, Propylene Glycol, Hydroxypropyl Methylcellulose, Diazolidinyl Urea, Fragrance, PEG-20 Sorbitan Stearate, Triethanolamine, Menthol, Iodopropynyl Butylcarbamate

Principal Display Panel - Bottle Label

NDC: 65517-1010-1

DawnMist®

DEODORANTS

Roll-On
Antiperspirant

REDUCES WETNESS & ODOR

FRESH SCENT

1.5 FL. OZ. (44ml)

INGREDIENTS AND APPEARANCE

DAWNMIST ANTIPERSPIRANT DEODORANT 
aluminum chlorohydrate lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65517-1010
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)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
HYPROMELLOSES (UNII: 3NXW29V3WO)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
TROLAMINE (UNII: 9O3K93S3TK)
MENTHOL (UNII: L7T10EIP3A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65517-1010-1	44 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	01/10/2013	09/28/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	01/10/2013	09/28/2021

Labeler - Dukal Corporation (791014871)

Establishment
Name	Address	ID/FEI	Business Operations
KEN PRIMA COSMECEUTICALS SDN. BHD.		865792209	manufacture(65517-1010)