AXE PHOENIX ANTIPERSPIRANT- aluminum zirconium tetrachlorohydrex gly 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 PHOENIX ANTIPERSPIRANT - aluminum zirconium tetrachlorohydrex gly stick

ACTIVE INGREDIENT

Active ingredient

Aluminum Zirconium Tetrachlorohydrex GLY(18.2%)

PURPOSE

Purposeanti-perspirant

INDICATIONS & USAGE

Uses
·reduces underarm wetness
·24 hour protection

WARNINGS

Warnings
For external use only

Do not use on broken skin

Ask a doctor before use if you havekidney disease

Stop useif rash or irritation occurs

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions
· apply to underarms only
·turn dial to raise product
·to ensure product appears clear on skin, do not overapply
·replace cap

INACTIVE INGREDIENT

Inactive ingredients

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

QUESTIONS

Questions?

Call toll-free 1-800-450-7580

Package

INGREDIENTS AND APPEARANCE

AXE  PHOENIX ANTIPERSPIRANT
aluminum zirconium tetrachlorohydrex gly stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64942-2352
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	18.2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
PPG-14 BUTYL ETHER (UNII: R199TJT95T)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
PEG-8 DISTEARATE (UNII: 7JNC8VN07M)
TALC (UNII: 7SEV7J4R1U)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64942-2352-1	76 g in 1 CONTAINER; Type 0: Not a Combination Product	09/02/2024
2	NDC: 64942-2352-3	14 g in 1 CONTAINER; Type 0: Not a Combination Product	09/02/2024
3	NDC: 64942-2352-2	48 g in 1 CONTAINER; Type 0: Not a Combination Product	09/02/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	09/02/2024

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