Axe Gold Dry Spray Antiperspirant

Manufacturer: Conopco Inc. d/b/a/ Unilever
Effective date: 2017-09-11
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:52:28

Label at a glance#

ProductAxe

Active ingredientALUMINUM CHLOROHYDRATE

Label structure10 sections

Indications and uses

reduces underarm wetness

Dosage and administration

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

Contacts and useful links#

PhoneLabel contact1-800-450-7580

Websitewww.inhalant.org

www.inhalant.org

Label contents#

Full prescribing information#

AXE GOLD DRY SPRAY ANTIPERSPIRANT - aluminum chlorohydrate aerosol, spray

DESCRIPTION SECTION

AXE GOLD DRY SPRAY ANTIPERSPIRANT

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient
Aluminum Chlorohydrate (20.2%)

Purpose

OTC - PURPOSE SECTION

antiperspirant

Uses

INDICATIONS & USAGE SECTION

reduces underarm wetness

Warnings

WARNINGS SECTION

• 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°F/50°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.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Questions?

OTC - QUESTIONS SECTION

Call toll-free 1-800-450-7580

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AxeGoldDrySprayAP

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
64942-1511-1	2020-01-31	C162847	48780-1	9d75b9d0-8d43-f424-e053-dadaa90a57ce	Axe Gold Dry Spray Antiperspirant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
64942-1511-1	Axe	107 g in 1 CAN	AEROSOL, SPRAY	107		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
64942-1511	AXE (GOLD DRY SPRAY ANTIPERSPIRANT) AEROSOL, SPRAY [CONOPCO INC. D/B/A/ UNILEVER]	1	Legacy NDC, 1 package rows	20170912_58ef2d15-10d1-1364-e053-2991aa0aba93.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

Axe
Gold Dry Spray Antiperspirant
BUTANE
ALUMINUM CHLOROHYDRATE
1,1-DIFLUOROETHANE
CYCLOMETHICONE 5
ISOBUTANE
PPG-14 BUTYL ETHER
PROPANE
PROPYLENE CARBONATE
DISTEARDIMONIUM HECTORITE
BUTYLATED HYDROXYTOLUENE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
64942-1511	64942-1511-1

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
Name	UNII	Kind
BUTANE	6LV4FOR43R	IACT
ALUMINUM CHLOROHYDRATE	HPN8MZW13M	ACTIB
1,1-DIFLUOROETHANE	0B1U8K2ME0	IACT
CYCLOMETHICONE 5	0THT5PCI0R	IACT
ISOBUTANE	BXR49TP611	IACT
PPG-14 BUTYL ETHER	R199TJT95T	IACT
PROPANE	T75W9911L6	IACT
PROPYLENE CARBONATE	8D08K3S51E	IACT
DISTEARDIMONIUM HECTORITE	X687XDK09L	IACT
BUTYLATED HYDROXYTOLUENE	1P9D0Z171K	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
58ef2d15-10d2-1364-e053-2991aa0aba93			58ef2d15-10d1-1364-e053-2991aa0aba93	2017-09-11	Warnings	Exact identifier spl id: 58ef2d15-10d2-1364-e053-2991aa0aba93 spl set id: 58ef2d15-10d1-1364-e053-2991aa0aba93

Reported adverse events (FAERS/openFDA)#

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