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DawnMist Antiperspirant Deodorant

Medically reviewed on Mar 21, 2018

Dosage form: liquid
Ingredients: ALUMINUM CHLOROHYDRATE 79mg in 1mL
Labeler: Dukal Corporation
NDC Code: 65517-1002

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.

DawnMist Antiperspirant Deodorant

Active Ingredient

Aluminum Chlorohydrate 7.90%

Purpose

Antiperspirant

UseReduces 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.

When using this product

■ Keep away from face and mouth ■ Do not spray near flames

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. Hold two inches from underarm and spray. Use daily for best results

Inactive Ingredients

Water, Alcohol, Glycerin, PEG-40 Hydrogenated Castor Oil, Diazolidinyl Urea, Fragrance, Iodopropynyl Butylcarbamate

Package Label

DawnMist

Reduces Wetness and Odor

Clean Fresh Scent

Antiperspirant Deodorant Spray

2 FL. OZ. (59ml)

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



DAWNMIST ANTIPERSPIRANT DEODORANT 
aluminum chlorohydrate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65517-1002
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM CHLOROHYDRATE (ALUMINUM CHLOROHYDRATE) ALUMINUM CHLOROHYDRATE79 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
ALCOHOL 
GLYCERIN 
POLYOXYL 40 HYDROGENATED CASTOR OIL 
DIAZOLIDINYL UREA 
IODOPROPYNYL BUTYLCARBAMATE 
Packaging
#Item CodePackage Description
1NDC:65517-1002-159 mL in 1 BOTTLE, PUMP
2NDC:65517-1002-2118 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35001/10/2013
Labeler - Dukal Corporation (791014871)

 
Dukal Corporation

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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