FDA.reportPublic FDA data

Axe

Manufacturer
Conopco Inc. d/b/a Unilever | Unilever Raeford HPCNA | Zolberg Corporation
Effective date
2015-07-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:44:15

Label at a glance#

ProductAxe Adrenaline Antiperspirant
Active ingredientAluminum Zirconium Tetrachlorohydrex GLY
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Aluminum Zirconium Tetrachlorohydrex GLY(19.0%)

OTC - PURPOSE SECTION

Purpose

antiperspirant

INDICATIONS & USAGE SECTION

Uses
· reduces underarm wetness

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

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Cyclopentasiloxane, Stearyl Alcohol, PPG-14 Butyl Ether, Hydrogenated Castor Oil, Talc, PEG-8 Distearate, Fragrance(Parfum), Sodium Starch Octenylsuccinate, Maltodextrin, Hydrolyzed Corn Starch, BHT, Silica

OTC - QUESTIONS SECTION

Questions?

Call toll-free 1-800-450-7580

2.7 oz PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AxeAdrenalinePDPAxeAdrenalinePDP

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64942-1423-12020-01-31C16284748780-19d75b9cf-f548-f424-e053-dadaa90a57ceAxe Adrenaline Antiperspirant Deodorant
64942-1423-22020-01-31C16284748780-19d75b9cf-f548-f424-e053-dadaa90a57ceAxe Adrenaline Antiperspirant Deodorant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1423-1Axe Adrenaline Antiperspirant76 g in 1 CONTAINERSTICK761
64942-1423-2Axe Adrenaline Antiperspirant14 g in 1 CONTAINERSTICK141

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1423AXE ADRENALINE ANTIPERSPIRANT (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY) STICK [CONOPCO INC. D/B/A UNILEVER]1Legacy NDC, 2 package rows20151201_81937bef-857f-4b29-9171-fa4e8b58f04e.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
64942-142364942-1423-1, 64942-1423-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
Aluminum Zirconium Tetrachlorohydrex GLY8O386558JEACTIB
CYCLOMETHICONE 50THT5PCI0RIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
STEARYL ALCOHOL2KR89I4H1YIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
TALC7SEV7J4R1UIACT
PEG-8 DISTEARATE7JNC8VN07MIACT
MALTODEXTRIN7CVR7L4A2DIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
SILICON DIOXIDEETJ7Z6XBU4IACT

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
8f026922-5ba1-43da-ba26-24fea4e9ebb081937bef-857f-4b29-9171-fa4e8b58f04e2015-07-23WarningsExact identifier
spl id: 8f026922-5ba1-43da-ba26-24fea4e9ebb0
spl set id: 81937bef-857f-4b29-9171-fa4e8b58f04e

Reported adverse events (FAERS/openFDA)#

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