FDA.reportPublic FDA data

Axe

Manufacturer
Conopco Inc. d/b/a/ Unilever
Effective date
2024-02-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:09:12

Label at a glance#

ProductAxe
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure10 sections

Indications and uses

reduces underarm wetness

Dosage and administration

apply to underarms only

Label contents#

Full prescribing information#

AXE ESSENCE BLACK PEPPER & CEDARWOOD 48H ANTIPERSPIRANT - aluminum zirconium tetrachlorohydrex gly stick

DESCRIPTION SECTION

Axe Dark Temptation 48H Anti Sweat Antiperspirant

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

Warnings

WARNINGS SECTION

For externaluse only

Do not use on broken skin

Stop use if rash or irritation occurs
Ask a doctor before use if you have kidney disease

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

PPG-14 Butyl Ether, Cyclopentasiloxane, Stearyl Alcohol, Isopropyl Palmitate, Mineral Oil, Hydrogenated Castor Oil, PEG-8 Distearate, Fragrance (Parfum), Polyethylene, BHT, Alpha-Isomethyl Ionone, Benzyl Alcohol, Benzyl Salicylate, Citronellol, Coumarin, Eugenol, Geraniol, Hexyl Cinnamal, Limonene, Linalool

Questions?

OTC - QUESTIONS SECTION

Call toll-free 1-800-450-7580

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Axe Essence AP ISAxe Essence AP IS

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-2266-1Axe76 g in 1 CONTAINERSTICK761
64942-2266-2Axe2 in 1 PACKAGESTICK21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-2266AXE (ESSENCE BLACK PEPPER AND CEDARWOOD 48H ANTIPERSPIRANT) STICK [CONOPCO INC. D/B/A/ UNILEVER]1Current NDC, 2 package rows20240301_12489124-e31e-80b0-e063-6394a90a06e0.zip

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-226664942-2266-1, 64942-2266-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
LIMONENE, (+)-GFD7C86Q1WIACT
GERANIOLL837108USYIACT
CYCLOMETHICONE 50THT5PCI0RIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
STEARYL ALCOHOL2KR89I4H1YIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
MINERAL OILT5L8T28FGPIACT
PEG-8 DISTEARATE7JNC8VN07MIACT
ISOPROPYL PALMITATE8CRQ2TH63MIACT
HIGH DENSITY POLYETHYLENEUG00KM4WR7IACT
LINALOOL, (+/-)-D81QY6I88EIACT
COUMARINA4VZ22K1WTIACT
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT
BENZYL ALCOHOLLKG8494WBHIACT
BENZYL SALICYLATEWAO5MNK9TUIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
EUGENOL3T8H1794QWIACT

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
AxeESSENCE BLACK PEPPER AND CEDARWOOD 48H ANTIPERSPIRANTConopco Inc. d/b/a/ Unilever12489124-e31e-80b0-e063-6394a90a06e02024-02-26WarningsExact identifier
ndc (package): 64942-2266-2
ndc (package): 64942-2266-1
ndc (product): 64942-2266
ndc11 (package): 64942226601
ndc11 (package): 64942226602
spl id: 1248846e-4fb0-84d3-e063-6394a90aa959
spl set id: 12489124-e31e-80b0-e063-6394a90a06e0

Reported adverse events (FAERS/openFDA)#

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