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Axe Phoenix Antiperspirant and Deodorant

Medically reviewed on June 12, 2018

Dosage form: stick
Ingredients: ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY 18.2g in 100g
Labeler: Conopco Inc. d/b/a/ Unilever
NDC Code: 64942-1539

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 Phoenix Antiperspirant and Deodorant

AXE PHOENIX ANTIPERSPIRANT AND DEODORANT - aluminum zirconium tetrachlorohydrex gly stick

Axe Phoenix Antiperspirant and Deodorant

Drug Facts

Active ingredient

Aluminum Zirconium Tetrachlorohydrex GLY (18.2 %)

Purpose

antiperspirant

Uses

• reduces underarm wetness

• 24 Hour Protection

Warnings

• For external use only.
• Do not use on broken skin .
• Ask a doctor before use if you have
kidney disease.
• Stop use if rash or irritation occurs.

• Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

apply to underarms only

Inactive ingredients

Cyclopentasiloxane, Stearyl Alcohol, PPG-14 Butyl Ether, Hydrogenated Castor Oil, Talc, PEG-8 Distearate, Fragrance (Parfum), BHT.

Questions?

Call toll-free 1-800-450-7580

Packaging

AXE  PHOENIX ANTIPERSPIRANT AND DEODORANT
aluminum zirconium tetrachlorohydrex gly stick
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1539
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY) ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY18.2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
PEG-8 DISTEARATE 
TALC 
CYCLOMETHICONE 5 
HYDROGENATED CASTOR OIL 
BUTYLATED HYDROXYTOLUENE 
PPG-14 BUTYL ETHER 
STEARYL ALCOHOL 
Packaging
#Item CodePackage Description
1NDC:64942-1539-176 g in 1 CONTAINER
2NDC:64942-1539-22 CONTAINER in 1 PACKAGE
2NDC:64942-1539-176 g in 1 CONTAINER
3NDC:64942-1539-348 g in 1 CONTAINER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35009/27/2017
Labeler - Conopco Inc. d/b/a/ Unilever (001375088)

 
Conopco Inc. d/b/a/ Unilever

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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