FDA.reportPublic FDA data

Axe

Manufacturer
Conopco d/b/a Unilever
Effective date
2025-07-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:12:14

Label at a glance#

ProductAxe
Active ingredientALUMINUM SESQUICHLOROHYDRATE
Label structure10 sections

Label contents#

Full prescribing information#

DESCRIPTION SECTION

Axe Black Vanilla Orange and Sandalwood Long Lasting Premium Scent Premium Antiperspirant

OTC - ACTIVE INGREDIENT SECTION

Aluminum Sesquichlorohydrate 9.6%

OTC - PURPOSE SECTION

Antiperspirant

INDICATIONS & USAGE SECTION

apply to underarms only

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

DOSAGE & ADMINISTRATION SECTION

apply to underarms only

INACTIVE INGREDIENT SECTION

Cyclopentasiloxane,Stearyl Alcohol,C12-15 Alkyl Benzoate,PPG-14 Butyl Ether,Hydrogenated Castor Oil,Glycine,PEG-8,Fragrance (Parfum), Calcium Chloride,Dimethicone,Polyethylene,Silica,Helianthus Annuus (Sunflower) Seed Oil,Steareth-100,Stearic Acid,BHT,Alpha-Isomethyl Ionone,Citral,Citronellol,Coumarin,Eugenol,Geraniol,Limonene,Linalool

OTC - QUESTIONS SECTION

call 1-800-761-3683

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-2379-1Axe74 g in 1 CONTAINERSTICK741

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-237964942-2379-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

Name, UNII, Kind table
NameUNIIKind
SILICAETJ7Z6XBU4IACT
ALPHA-ISOMETHYL IONONE9XP4LC555BIACT
GLYCINETE7660XO1CIACT
PEG-8B697894SGQIACT
DIMETHICONE92RU3N3Y1OIACT
STEARETH-1004OH5W9UM87IACT
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL3W1JG795YIIACT
EUGENOL3T8H1794QWIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
POLYETHYLENEUG00KM4WR7IACT
LINALOOLD81QY6I88EIACT
STEARYL ALCOHOL2KR89I4H1YIACT
CITRONELLOLP01OUT964KIACT
GERANIOLL837108USYIACT
ALUMINUM SESQUICHLOROHYDRATEUCN889409VACTIB
HYDROGENATED CASTOR OILZF94AP8MEYIACT
COUMARINA4VZ22K1WTIACT
LIMONENE, (+)-GFD7C86Q1WIACT
CITRALT7EU0O9VPPIACT
BHT1P9D0Z171KIACT
CYCLOPENTASILOXANE0THT5PCI0RIACT
C12-15 ALKYL BENZOATEA9EJ3J61HQIACT
CALCIUM CHLORIDEM4I0D6VV5MIACT
STEARIC ACID4ELV7Z65APIACT

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
AxeBLACK VANILLA ORANGE AND SANDALWOOD LONG LASTING PREMIUM SCENT PREMIUM ANTIPERSPIRANTConopco d/b/a Unilever3a35cf1a-073f-6c27-e063-6394a90a024c2025-07-18WarningsExact identifier
ndc (package): 64942-2379-1
ndc (product): 64942-2379
ndc11 (package): 64942237901
spl id: 3a35cf1a-0740-6c27-e063-6394a90a024c
spl set id: 3a35cf1a-073f-6c27-e063-6394a90a024c

Reported adverse events (FAERS/openFDA)#

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