Axe Signature Night Dry Spray Antiperspirant

Manufacturer
Conopco Inc. d/b/a Unilever
Effective date
2020-09-30
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:30:35

Label at a glance#

ProductAxe Signature Night Antiperspirant
Active ingredientALUMINUM CHLOROHYDRATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Aluminum chlorohydrate (23.3%)

OTC - PURPOSE SECTION

Purpose

anti-perspirant

INDICATIONS & USAGE SECTION

Uses
· reduces underarm wetness

WARNINGS SECTION

WARNINGS

For external use only

• FLAMMABLE.  DO NOT USE NEAR HEAT, FLAME OR WHILE SMOKING.  CAN CAUSE SERIOUS INJURY OR DEATH.
• Keep away from face and mouth to avoid breathing in.
• Avoid spraying in eyes. Contents under pressure. Do not puncture or incinerate. Do not expose to heat or store at temperatures above 120 degrees F/50 degrees C or in enclosed places that could overheat.
• Do not use on broken skin. Stop use if rash or irritation occurs.
• Ask a doctor before using if you have kidney disease.
• USE ONLY AS DIRECTED.  INTENTIONAL MISUSE BY DELIBERATELY CONCENTRATING  AND INHALING THE CONTENTS CAN BE HARMFUL OR FATAL. Help stop inhalation abuse.  For information visit www.inhalant.org

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• KEEP OUT OF REACH OF CHILDREN

DOSAGE & ADMINISTRATION SECTION

Directions  Apply to underarms only.  If dispenser clogs, rinse in warm water.

INACTIVE INGREDIENT SECTION

Inactive ingredients

Butane, Cyclopentasiloxane, Hydrofluorocarbon 152a, Isobutane, PPG-14 Butyl Ether, Fragrance (Parfum), Disteardimonium Hectorite, Propane, BHT, Propylene Carbonate

OTC - QUESTIONS SECTION

Questions?
Call toll-free 1-800-450-7580

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AxeNightDrySprayAxeNightDrySpray

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1403-1AxeSignature Night Antiperspirant107 g in 1 CANAEROSOL, SPRAY1073
64942-1403-2AxeSignature Night Antiperspirant28 g in 1 CANAEROSOL, SPRAY283

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1403AXE SIGNATURE NIGHT ANTIPERSPIRANT (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [CONOPCO INC. D/B/A UNILEVER]3Legacy NDC, 2 package rows20201001_4062c119-6b07-4ccf-a564-3cc164bd42fd.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
64942-140364942-1403-1, 64942-1403-2

Ingredients#

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

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

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
b091d362-c64b-c485-e053-2995a90a2a924062c119-6b07-4ccf-a564-3cc164bd42fd2020-09-30WarningsExact identifier
spl id: b091d362-c64b-c485-e053-2995a90a2a92
spl set id: 4062c119-6b07-4ccf-a564-3cc164bd42fd

Reported adverse events (FAERS/openFDA)#

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