FDA.reportPublic FDA data

Axe

Manufacturer
Conopco Inc. d/b/a/ Unilever
Effective date
2024-11-06
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:34:41

Label at a glance#

ProductAxe
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure9 sections

Indications and uses

reduces underarm wetness

Dosage and administration

apply to underarms only

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Aluminum Zirconium Tetrachlorohydrex GLY (19.0 %)

Purpose

OTC - PURPOSE SECTION

antiperspirant

Uses

INDICATIONS & USAGE SECTION

reduces underarm wetness

Warnings

WARNINGS SECTION

• For externaluse 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

Isopropyl Palmitate, Stearyl Alcohol, Cyclopentasiloxane, PPG-14 Butyl Ether, Mineral Oil, Talc, Hydrogenated Castor Oil, Fragrance (Parfum), Steareth-100, BHT, Coumarin, Limonene, Linalool

Questions?

OTC - QUESTIONS SECTION

Call toll-free 1-800-450-7580

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Axe Dark Temptation AP ISAxe Dark Temptation AP IS

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
594e2c86-3079-4e6e-96c9-48f7a8afc78dProduct name120230718

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-2183-1Axe76 g in 1 CONTAINERSTICK763
64942-2183-2Axe2 in 1 CONTAINERSTICK23
64942-2183-3Axe2 in 1 CONTAINERSTICK23
64942-2183-4Axe48 g in 1 CONTAINERSTICK483

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-2183AXE (DARK TEMPTATION DARK CHOCOLATE 48H SWEAT AND ODOR PROTECTION ANTIPERSPIRANT) STICK [CONOPCO INC. D/B/A/ UNILEVER]3Current NDC, 4 package rows20241108_04377fa2-7d05-503b-e063-6394a90a0a42.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-218364942-2183-1, 64942-2183-2, 64942-2183-3, 64942-2183-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
ISOPROPYL PALMITATE8CRQ2TH63MIACT
TALC7SEV7J4R1UIACT
CYCLOMETHICONE 50THT5PCI0RIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
STEARYL ALCOHOL2KR89I4H1YIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
MINERAL OILT5L8T28FGPIACT
STEARETH-1004OH5W9UM87IACT
LIMONENE, (+)-GFD7C86Q1WIACT
LINALOOL, (+/-)-D81QY6I88EIACT
COUMARINA4VZ22K1WTIACT

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
AxeDARK TEMPTATION DARK CHOCOLATE 48H SWEAT AND ODOR PROTECTION ANTIPERSPIRANTConopco Inc. d/b/a/ Unilever04377fa2-7d05-503b-e063-6394a90a0a422024-11-06WarningsExact identifier
ndc (package): 64942-2183-1
ndc (package): 64942-2183-3
ndc (package): 64942-2183-2
ndc (package): 64942-2183-4
ndc (product): 64942-2183
ndc11 (package): 64942218304
ndc11 (package): 64942218303
ndc11 (package): 64942218301
ndc11 (package): 64942218302
spl id: 26473383-282b-fb10-e063-6394a90a5fa2
spl set id: 04377fa2-7d05-503b-e063-6394a90a0a42

Reported adverse events (FAERS/openFDA)#

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