Axe

Manufacturer: Conopco Inc. d/b/a/ Unilever
Effective date: 2021-12-01
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:45:17

Label at a glance#

ProductAxe Apollo Antiperspirant and Deodorant

Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY

Label structure10 sections

Indications and uses

• reduces underarm wetness • 24 Hour Protection

Dosage and administration

apply to underarms only

Contacts and useful links#

PhoneLabel contact1-800-450-7580

Label contents#

Full prescribing information#

AXE APOLLO ANTIPERSPIRANT AND DEODORANT - aluminum zirconium tetrachlorohydrex gly stick

DESCRIPTION SECTION

Axe Apollo Antiperspirant and Deodorant

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Aluminum Zirconium Tetrachlorohydrex GLY (18.2 %)

Purpose

OTC - PURPOSE SECTION

antiperspirant

Uses

INDICATIONS & USAGE SECTION

• reduces underarm wetness

• 24 Hour Protection

Warnings

WARNINGS SECTION

• 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

apply to underarms only

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Questions?

OTC - QUESTIONS SECTION

Call toll-free 1-800-450-7580

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AxeApolloAPDeo

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
64942-1532-1	2025-01-30	C162847	48780-1	9d75b9d0-344b-f424-e053-dadaa90a57ce	Axe Apollo Antiperspirant and Deodorant
64942-1532-2	2025-01-30	C162847	48780-1	9d75b9d0-344b-f424-e053-dadaa90a57ce	Axe Apollo Antiperspirant and Deodorant
64942-1532-1	2021-12-01	C162847	48780-1	9d75b9d0-344b-f424-e053-dadaa90a57ce	Axe Apollo Antiperspirant and Deodorant
64942-1532-2	2021-12-01	C162847	48780-1	9d75b9d0-344b-f424-e053-dadaa90a57ce	Axe Apollo Antiperspirant and Deodorant
64942-1532-1	2020-01-31	C162847	48780-1	9d75b9d0-344b-f424-e053-dadaa90a57ce	Axe Apollo Antiperspirant and Deodorant
64942-1532-2	2020-01-31	C162847	48780-1	9d75b9d0-344b-f424-e053-dadaa90a57ce	Axe Apollo Antiperspirant and Deodorant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
64942-1532-1	AxeApollo Antiperspirant and Deodorant	76 g in 1 CONTAINER	STICK	76		2
64942-1532-2	AxeApollo Antiperspirant and Deodorant	2 in 1 PACKAGE	STICK	2		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
64942-1532	AXE APOLLO ANTIPERSPIRANT AND DEODORANT (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY) STICK [CONOPCO INC. D/B/A/ UNILEVER]	2	Legacy NDC, 2 package rows	20211202_59b86f6e-7c04-2dbc-e053-2a91aa0a792c.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

Axe Apollo Antiperspirant and Deodorant
Aluminum Zirconium Tetrachlorohydrex GLY
PEG-8 DISTEARATE
TALC
CYCLOMETHICONE 5
HYDROGENATED CASTOR OIL
BUTYLATED HYDROXYTOLUENE
PPG-14 BUTYL ETHER
STEARYL ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
64942-1532	64942-1532-1, 64942-1532-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PEG-8 DISTEARATE	7JNC8VN07M	IACT
TALC	7SEV7J4R1U	IACT
CYCLOMETHICONE 5	0THT5PCI0R	IACT
HYDROGENATED CASTOR OIL	ZF94AP8MEY	IACT
BUTYLATED HYDROXYTOLUENE	1P9D0Z171K	IACT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY	8O386558JE	ACTIB
PPG-14 BUTYL ETHER	R199TJT95T	IACT
STEARYL ALCOHOL	2KR89I4H1Y	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
d2191165-7f49-687c-e053-2a95a90a37b3			59b86f6e-7c04-2dbc-e053-2a91aa0a792c	2021-12-01	Warnings	Exact identifier spl id: d2191165-7f49-687c-e053-2a95a90a37b3 spl set id: 59b86f6e-7c04-2dbc-e053-2a91aa0a792c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.