AXE PHOENIX 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 Phoenix Antiperspirant and Deodorant

AXE PHOENIX ANTIPERSPIRANT AND DEODORANT - aluminum zirconium tetrachlorohydrex gly stick

Axe Phoenix Antiperspirant and Deodorant

Drug Facts

Active ingredient

Aluminum Zirconium Tetrachlorohydrex GLY (18.2 %)

Purpose

antiperspirant

Uses

• reduces underarm wetness

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

Questions?

Call toll-free 1-800-450-7580

Packaging

AxePhoenixAPDeo

AXE PHOENIX ANTIPERSPIRANT AND DEODORANT
aluminum zirconium tetrachlorohydrex gly stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:64942-1539
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE) (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY - UNII:8O386558JE)	ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY	18.2 g in 100 g

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

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:64942-1539-1	76 g in 1 CONTAINER; Type 0: Not a Combination Product	09/27/2017
2	NDC:64942-1539-2	2 in 1 PACKAGE	09/27/2017
2	NDC:64942-1539-1	76 g in 1 CONTAINER; Type 0: Not a Combination Product
3	NDC:64942-1539-3	48 g in 1 CONTAINER; Type 0: Not a Combination Product	06/12/2018

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part350	09/27/2017

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