DAWNMIST ANTIPERSPIRANT DEODORANT  - aluminum chlorohydrate liquid 
Dukal Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Active Ingredient

Aluminum Chlorohydrate 7.80%

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, Polysorbate 60, Glycerin, PEG-100 Stearate, Sorbitan Stearate, Cetearyl Alcohol, Dimethicone, Magnesium Aluminum Silicate, Glyceryl Stearate, Hydroxyethylcellulose, Sodium Benzoate,
Methylparaben, Disodium EDTA, Propylparaben

Package Label

DawnMist

Reduces Wetness and Odor

Unscented

Roll-On Antiperspirant Deodorant Spray

2 FL. OZ. (59ml)

Manufactured for:
DUKAL CORPORATION
Ronkonkoma, NY 11779
(631) 656-3800
www.dukal.com

label


DAWNMIST ANTIPERSPIRANT DEODORANT  
aluminum chlorohydrate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65517-1011
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM CHLOROHYDRATE (ALUMINUM CHLOROHYDRATE) ALUMINUM CHLOROHYDRATE78 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
MINERAL OIL 
POLYSORBATE 60 
GLYCERIN 
PEG-100 STEARATE 
SORBITAN MONOSTEARATE 
CETOSTEARYL ALCOHOL 
MAGNESIUM ALUMINUM SILICATE 
GLYCERYL MONOSTEARATE 
SODIUM BENZOATE 
METHYLPARABEN 
EDETATE DISODIUM 
PROPYLPARABEN 
Packaging
#Item CodePackage Description
1NDC:65517-1011-159 mL in 1 BOTTLE, WITH APPLICATOR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35001/10/2013
Labeler - Dukal Corporation (791014871)

Revised: 03/2013
Document Id: 12d17f42-c6f4-4e58-8fb2-3a6e38e79af8
Set id: 70302841-5525-4060-ad26-47e18b43742b
Version: 4
Effective Time: 20130321
 
Dukal Corporation