AXE- black 48h fresh and dry antiperspirant stick 
Conopco Inc. d/b/a/ Unilever

----------

Axe Black 48H Fresh & Dry Antiperspirant

AXE BLACK 48H FRESH & DRY ANTIPERSPIRANT - aluminum zirconium tetrachlorohydrex gly stick

Axe Black 48H Anti Sweat Antiperspirant

Drug Facts

Active ingredient

Aluminum Zirconium Tetrachlorohydrex GLY (19.0 %)

Purpose

antiperspirant

Uses

• reduces underarm wetness

• 48 Hour Protection

Warnings

• For externaluse 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

Isopropyl Palmitate, Stearyl Alcohol, Cyclopentasiloxane, PPG-14 Butyl Ether, Mineral Oil, Talc, Hydrogenated Castor Oil, Fragrance (Parfum), Steareth-100, BHT.

Questions?

Call toll-free 1-800-450-7580

Axe Black AP Stick

AXE 
black 48h fresh and dry antiperspirant stick
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-2070
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 GLY19 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
TALC (UNII: 7SEV7J4R1U)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
PPG-14 BUTYL ETHER (UNII: R199TJT95T)  
MINERAL OIL (UNII: T5L8T28FGP)  
STEARETH-100 (UNII: 4OH5W9UM87)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:64942-2070-176 g in 1 CONTAINER; Type 0: Not a Combination Product10/22/2022
2NDC:64942-2070-22 in 1 PACKAGE10/22/2022
2NDC:64942-2070-176 g in 1 CONTAINER; Type 0: Not a Combination Product
3NDC:64942-2070-32 in 1 PACKAGE10/22/2022
3NDC:64942-2070-22 in 1 PACKAGE
3NDC:64942-2070-176 g in 1 CONTAINER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01910/22/2022
Labeler - Conopco Inc. d/b/a/ Unilever (001375088)

Revised: 11/2024
Document Id: 264824a1-103e-9bcd-e063-6394a90a2211
Set id: e38e3d5e-4da1-7e94-e053-2995a90a8d1a
Version: 2
Effective Time: 20241106
 
Conopco Inc. d/b/a/ Unilever