AXE- black chill antiperspirant and deodorant 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 Black Chill 48H Dry Antiperspirant and Deodorant

AXE BLACK CHILL 48H DRY ANTIPERSPIRANT AND DEODORANT - aluminum zirconium tetrachlorohydrex gly stick

Axe Black Chill 48H Dry Antiperspirant and Deodorant

Drug Facts

Active ingredient

Aluminum Zirconium Tetrachlorohydrex GLY (18.2 %)

Purpose

antiperspirant

Uses

• reduces underarm wetness

• 48 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, Isopropyl Palmitate, Stearyl Alcohol, Mineral Oil, Talc, Hydrogenated Castor Oil, Fragrance (Parfum), Steareth-100, BHT.

Questions?

Call toll-free 1-800-450-7580

Packaging

AxeBlackChillAPDeo

AXE 
black chill antiperspirant and deodorant stick
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1590
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 GLY18.2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
TALC (UNII: 7SEV7J4R1U)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
MINERAL OIL (UNII: T5L8T28FGP)  
STEARETH-100 (UNII: 4OH5W9UM87)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:64942-1590-176 g in 1 CONTAINER; Type 0: Not a Combination Product01/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35001/01/2020
Labeler - Conopco Inc. d/b/a/ Unilever (001375088)

Revised: 11/2020
Document Id: b3a2f215-c295-85c9-e053-2995a90a6944
Set id: 72c562d9-f5fc-c3cd-e053-2a91aa0ad648
Version: 2
Effective Time: 20201108
 
Conopco Inc. d/b/a/ Unilever