AXE SIGNATURE NIGHT ANTIPERSPIRANT- 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 - Signature Night Antiperspirant

Drug Facts

Active ingredient

Aluminum Zirconium Tetrachlorohydrex GLY(11.4%)

Purpose

antiperspirant

Uses

• reduces underarm wetness

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

Questions?

Call toll-free 1-800-450-7580

48 HR ANTI MARKS PROTECTION
ANTI WHITE MARKS
ANTI YELLOW STAINS
AXE NIGHT 48HR ANTI MARKS PROTECTION.
KEEPS YOU (AND YOUR SHIRTS) FEELING CLEAN AND FRESH.

Packaging

AxeNightAPBKLabel AxeNightAPFTLabel image description

AXE SIGNATURE NIGHT ANTIPERSPIRANT
aluminum zirconium tetrachlorohydrex gly stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:64942-1474
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	11.4 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
PPG-14 BUTYL ETHER (UNII: R199TJT95T)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
PEG-8 DISTEARATE (UNII: 7JNC8VN07M)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:64942-1474-1	76 g in 1 CONTAINER; Type 0: Not a Combination Product	10/19/2016
2	NDC:64942-1474-2	14 g in 1 CONTAINER; Type 0: Not a Combination Product	10/19/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part350	10/19/2016

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