FDA.reportPublic FDA data

Axe

Manufacturer
Conopco Inc. d/b/a/ Unilever
Effective date
2020-11-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:33:15

Label at a glance#

ProductAxe
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure10 sections

Indications and uses

• reduces underarm wetness • 48 Hour Protection

Dosage and administration

apply to underarms only

Label contents#

Full prescribing information#

AXE ESSENCE 48H DRY ANTIPERSPIRANT AND DEODORANT - aluminum zirconium tetrachlorohydrex gly stick

DESCRIPTION SECTION

Axe Essence 48H Dry 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

• 48 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, Isopropyl Palmitate, Stearyl Alcohol, Mineral Oil, Talc, Hydrogenated Castor Oil, Fragrance (Parfum), Steareth-100, BHT.

Questions?

OTC - QUESTIONS SECTION

Call toll-free 1-800-450-7580

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AxeEssenceAPDeoAxeEssenceAPDeo

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64942-1598-12025-01-30C16284748780-19d75b9d1-12b4-f424-e053-dadaa90a57ceAxe Essence 48H Dry Antiperspirant and Deodorant
64942-1598-12020-11-08C16284748780-19d75b9d1-12b4-f424-e053-dadaa90a57ceAxe Essence 48H Dry Antiperspirant and Deodorant
64942-1598-12020-01-31C16284748780-19d75b9d1-12b4-f424-e053-dadaa90a57ceAxe Essence 48H Dry Antiperspirant and Deodorant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1598-1Axe76 g in 1 CONTAINERSTICK763

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1598AXE (ESSENCE ANTIPERSPIRANT AND DEODORANT) STICK [CONOPCO INC. D/B/A/ UNILEVER]3Legacy NDC, 1 package rows20201110_72c84cb4-378d-2d33-e053-2a91aa0af19e.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-159864942-1598-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
TALC7SEV7J4R1UIACT
CYCLOMETHICONE 50THT5PCI0RIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
STEARYL ALCOHOL2KR89I4H1YIACT
ISOPROPYL PALMITATE8CRQ2TH63MIACT
MINERAL OILT5L8T28FGPIACT
STEARETH-1004OH5W9UM87IACT

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
b3a32670-6cc3-22d3-e053-2995a90a7ccf72c84cb4-378d-2d33-e053-2a91aa0af19e2020-11-08WarningsExact identifier
spl id: b3a32670-6cc3-22d3-e053-2995a90a7ccf
spl set id: 72c84cb4-378d-2d33-e053-2a91aa0af19e

Reported adverse events (FAERS/openFDA)#

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