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Axe by Conopco Inc. d/b/a/ Unilever

Dosage form: aerosol, spray
Ingredients: ALUMINUM CHLOROHYDRATE 23.3g in 100g
Labeler: Conopco Inc. d/b/a/ Unilever
NDC Code: 64942-1519

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.

Axe Night Dry Spray Antiperspirant

AXE NIGHT DRY SPRAY ANTIPERSPIRANT - aluminum chlorohydrate aerosol, spray

AXE NIGHT DRY SPRAY ANTIPERSPIRANT

Drug Facts

Active ingredient
Aluminum Chlorohydrate (23.3%)

Purpose

antiperspirant

Uses

reduces underarm wetness

Warnings

• For external use only

• FLAMMABLE. DO NOT USE NEAR HEAT, FLAME, OR WHILE SMOKING. CAN CAUSE SERIOUS INJURY OR DEATH
• Keep away from face and mouth to avoid breathing in.
• Avoid spraying in eyes. Contents under pressure. Do not puncture or incinerate. Do not expose to heat or store at temperatures above 120°F/50°C or in enclosed places that could overheat
• Do not use on broken skin. Stop use if rash or irritation occurs.
• Ask a doctor before using if you have kidney disease.
• USE ONLY AS DIRECTED. INTENTIONAL MISUSE BY DELIBERATELY CONCENTRATING AND INHALING THE CONTENTS CAN BE HARMFUL OR FATAL.


Help stop inhalation abuse. For information visit www.inhalant.org

• KEEP OUT OF REACH OF CHILDREN.

Directions

Apply to underarms only. If dispenser clogs, rinse in warm water

Inactive ingredients

Butane, Cyclopentasiloxane, Hydrofluorocarbon 152a, Isobutane, PPG-14 Butyl Ether, Fragrance (Parfum), Disteardimonium Hectorite, Propane, BHT, Propylene Carbonate.

Questions?

Call toll-free 1-800-450-7580

Packaging

AXE 
night dry spray antiperspirant aerosol, spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1519
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM CHLOROHYDRATE (ALUMINUM CHLOROHYDRATE) ALUMINUM CHLOROHYDRATE23.3 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
BUTANE 
1,1-DIFLUOROETHANE 
CYCLOMETHICONE 5 
ISOBUTANE 
PPG-14 BUTYL ETHER 
PROPANE 
PROPYLENE CARBONATE 
DISTEARDIMONIUM HECTORITE 
BUTYLATED HYDROXYTOLUENE 
Packaging
#Item CodePackage Description
1NDC:64942-1519-1107 g in 1 CAN
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35009/11/2017
Labeler - Conopco Inc. d/b/a/ Unilever (001375088)

 
Conopco Inc. d/b/a/ Unilever

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Medically reviewed on Sep 11, 2017

Further information

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

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