FDA.reportPublic FDA data

Axe

Manufacturer
Conopco Inc. d/b/a Unilever
Effective date
2022-11-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:51:35

Label at a glance#

ProductAxe Dry Phoenix
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Aluminum Zirconium Tetrachlorohydrex GLY(18.2%)

OTC - PURPOSE SECTION

Purposeanti-perspirant

INDICATIONS & USAGE SECTION

Uses

· reduces underarm wetness

· 24 hour protection

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
· turn dial to raise product
· to ensure product appears clear on skin, do not overapply
· replace cap

INACTIVE INGREDIENT SECTION

Inactive ingredients

Cyclopentasiloxane, PPG-14 Butyl Ether, Stearyl Alcohol, Hydrogenated Castor Oil, PEG-8 Distearate, Talc, Fragrance (Parfum), BHT.

OTC - QUESTIONS SECTION

Questions?

Call toll-free 1-800-450-7580

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Axe Dry Phoenix 2.7 PDPAxe Dry Phoenix 2.7 PDP

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64942-1164-62024-01-30C16284748780-11030e365-6ad0-111a-e063-dadaa90a10e2Axe Phoenix Antiperspirant Deodorant
64942-1164-82024-01-30C16284748780-11030e365-6ad0-111a-e063-dadaa90a10e2Axe Phoenix Antiperspirant Deodorant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1164-6AxeDry Phoenix48 g in 1 CONTAINERSTICK483
64942-1164-8AxeDry Phoenix14 g in 1 CONTAINERSTICK143

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1164AXE DRY PHOENIX (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY) STICK [CONOPCO INC. D/B/A UNILEVER]3Legacy NDC, 2 package rows20221117_ed88cf55-d947-2b83-e053-2a95a90ab1e8.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
64942-116464942-1164-6, 64942-1164-8

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

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
ed88cf6a-c365-d2ce-e053-2a95a90ae080ed88cf55-d947-2b83-e053-2a95a90ab1e82022-11-15WarningsExact identifier
spl id: ed88cf6a-c365-d2ce-e053-2a95a90ae080
spl set id: ed88cf55-d947-2b83-e053-2a95a90ab1e8

Reported adverse events (FAERS/openFDA)#

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