FDA.reportPublic FDA data

Axe

Manufacturer
Conopco, Inc. d/b/a/ Unilever
Effective date
2016-10-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:47:35

Label at a glance#

ProductAxe Black Antiperspirant
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure9 sections

Indications and uses

reduces underarm wetness • 24 hour Protection

Dosage and administration

apply to underarms only

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Zirconium Tetrachlorohydrex GLY (18.2%)

Purpose

OTC - PURPOSE SECTION

anti-perspirant

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

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64942-1463-12020-01-31C16284748780-19d75b9d0-8e36-f424-e053-dadaa90a57ceAXE Black Antiperspirant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1463-1AxeBlack Antiperspirant76 g in 1 CONTAINERSTICK761

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1463AXE BLACK ANTIPERSPIRANT (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY) STICK [CONOPCO, INC. D/B/A/ UNILEVER]1Legacy NDC, 1 package rows20161014_493ee634-e495-482b-a95d-202412e88aa3.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-146364942-1463-1

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
NameUNIIKind
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
CYCLOMETHICONE 50THT5PCI0RIACT
STEARYL ALCOHOL2KR89I4H1YIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
TALC7SEV7J4R1UIACT
PEG-8 DISTEARATE7JNC8VN07MIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
606ef165-fd77-4bb2-8882-97eaccf0115c493ee634-e495-482b-a95d-202412e88aa32016-10-13WarningsExact identifier
spl id: 606ef165-fd77-4bb2-8882-97eaccf0115c
spl set id: 493ee634-e495-482b-a95d-202412e88aa3

Reported adverse events (FAERS/openFDA)#

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