AXE- essence black pepper and cedarwood scent 48h fresh and dry antiperspirant stick

Axe by

Drug Labeling and Warnings

Axe by is a Otc medication manufactured, distributed, or labeled by Conopco Inc. d/b/a/ Unilever. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

AXE ESSENCE BLACK PEPPER & CEDARWOOD SCENT 48H FRESH & DRY ANTIPERSPIRANT - aluminum zirconium tetrachlorohydrex gly stick

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

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 1-800-761-3683

Packaging

INGREDIENTS AND APPEARANCE

AXE 
essence black pepper and cedarwood scent 48h fresh and dry antiperspirant stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64942-2122
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE) (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY - UNII:8O386558JE)	ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY	19 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
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)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64942-2122-1	76 g in 1 CONTAINER; Type 0: Not a Combination Product	07/19/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	07/03/2023

Labeler - Conopco Inc. d/b/a/ Unilever (001375088)