Axe

Manufacturer: Conopco Inc. d/b/a Unilever | Unilever Raeford HPCNA
Effective date: 2015-10-08
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 22:44:15

Label at a glance#

ProductAxe Dry Apollo Antiperspirant Deodorant

Active ingredientAluminum Zirconium Tetrachlorohydrex GLY

Label structure9 sections

Contacts and useful links#

PhoneLabel contact1-800-450-7580

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Aluminum Zirconium Tetrachlorohydrex GLY(18.2%)

OTC - PURPOSE SECTION

Purposeanti-perspirant

INDICATIONS & USAGE SECTION

Uses
· reduces underarm wetness
· 24 hour protection

WARNINGS SECTION

Warnings
For external use only

OTC - DO NOT USE SECTION

Do not use on broken skin

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have kidney disease

OTC - STOP USE SECTION

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.

DOSAGE & ADMINISTRATION SECTION

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

INACTIVE INGREDIENT SECTION

Inactive ingredients

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

OTC - QUESTIONS SECTION

Questions?

Call toll-free 1-800-450-7580

2.7 oz PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Axe Dry Apollo 2.7 PDP

Twin Sleeve

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AxeApollotwinsleeve

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
64942-1262-2	2020-01-31	C162847	48780-1	9d75b9d1-296a-f424-e053-dadaa90a57ce	Axe Dry Apollo Antiperspirant Deodorant
64942-1262-3	2020-01-31	C162847	48780-1	9d75b9d1-296a-f424-e053-dadaa90a57ce	Axe Dry Apollo Antiperspirant Deodorant
64942-1262-5	2020-01-31	C162847	48780-1	9d75b9d1-296a-f424-e053-dadaa90a57ce	Axe Dry Apollo Antiperspirant Deodorant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
64942-1262-1	Axe Dry Apollo Antiperspirant Deodorant	76 g in 1 CONTAINER	STICK	76	2
64942-1262-2	Axe Dry Apollo Antiperspirant Deodorant	48 g in 1 CONTAINER	STICK	48	2
64942-1262-3	Axe Dry Apollo Antiperspirant Deodorant	14 g in 1 CONTAINER	STICK	14	2
64942-1262-4	Axe Dry Apollo Antiperspirant Deodorant	2 in 1 CONTAINER	STICK	2	2
64942-1262-5	Axe Dry Apollo Antiperspirant Deodorant	2 in 1 CONTAINER	STICK	2	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
64942-1262	AXE DRY APOLLO ANTIPERSPIRANT DEODORANT (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY) STICK [CONOPCO INC. D/B/A UNILEVER]	2	Legacy NDC, 5 package rows	20151201_2deb3f7c-5b7d-4f3b-aae3-0af10e3e8ce6.zip

Products#

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

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
64942-1262	64942-1262-1, 64942-1262-4, 64942-1262-5, 64942-1262-2, 64942-1262-3

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
Aluminum Zirconium Tetrachlorohydrex GLY	8O386558JE	ACTIB
CYCLOMETHICONE 5	0THT5PCI0R	IACT
PPG-14 BUTYL ETHER	R199TJT95T	IACT
STEARYL ALCOHOL	2KR89I4H1Y	IACT
HYDROGENATED CASTOR OIL	ZF94AP8MEY	IACT
PEG-8 DISTEARATE	7JNC8VN07M	IACT
TALC	7SEV7J4R1U	IACT
BUTYLATED HYDROXYTOLUENE	1P9D0Z171K	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
04a3988c-d83d-435a-9ccc-06d80d76cab0			2deb3f7c-5b7d-4f3b-aae3-0af10e3e8ce6	2015-10-08	Warnings	Exact identifier spl id: 04a3988c-d83d-435a-9ccc-06d80d76cab0 spl set id: 2deb3f7c-5b7d-4f3b-aae3-0af10e3e8ce6

Reported adverse events (FAERS/openFDA)#

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