AXE NIGHT ANTIPERSPIRANT AND DEODORANT- aluminum zirconium tetrachlorohydrex gly stick 
Conopco, Inc. d/b/a/ Unilever

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.

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Axe Night Antiperspirant and Deodorant

AXE NIGHT ANTIPERSPIRANT AND DEODORANT - aluminum zirconium tetrachlorohydrex gly stick

Axe Night Antiperspirant and Deodorant

Drug Facts

Active ingredient


Aluminum Zirconium Tetrachlorohydrex GLY (11.4 %)

Purpose

antiperspirant

Uses

• reduces underarm wetness

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

Questions?

Call toll-free 1-800-450-7580

Packaging

AxeNightAPDeo

AXE  NIGHT ANTIPERSPIRANT AND DEODORANT
aluminum zirconium tetrachlorohydrex gly stick
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1542
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE) (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY - UNII:8O386558JE) ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY11.4 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
PPG-14 BUTYL ETHER (UNII: R199TJT95T)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
PEG-8 DISTEARATE (UNII: 7JNC8VN07M)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:64942-1542-176 g in 1 CONTAINER; Type 0: Not a Combination Product09/27/2017
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)

Revised: 12/2021
Document Id: d2193225-491e-4b3e-e053-2a95a90ad91b
Set id: 5a35075b-bcb0-ec7d-e053-2991aa0a4f6b
Version: 2
Effective Time: 20211201
 
Conopco, Inc. d/b/a/ Unilever