Indications and uses
reduces underarm wetness
Axe Phoenix Dry Spray Antiperspirant 48HR Protection Dry
- Manufacturer
- Conopco Inc. d/b/a/ Unilever
- Effective date
- 2021-12-01
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-05-31 23:45:21
Label at a glance#
ProductAxe
Active ingredientALUMINUM CHLOROHYDRATE
Label structure10 sections
Dosage and administration
Apply to underarms only. If dispenser clogs, rinse in warm water
Contacts and useful links#
Websitewww.inhalant.org
www.inhalant.org
www.inhalant.orgLabel contents#
Full prescribing information#
AXE PHOENIX DRY SPRAY ANTIPERSPIRANT 48HR PROTECTION DRY - aluminum chlorohydrate aerosol, spray
Axe Phoenix Dry Spray Antiperspirant 48HR Protection Dry
Drug Facts
Active ingredient
Aluminum Chlorohydrate (23.3%)
Purpose
antiperspirant
Uses
reduces underarm wetness
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°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
Apply to underarms only. If dispenser clogs, rinse in warm water
Inactive ingredients
Butane, Cyclopentasiloxane, Hydrofluorocarbon 152a, Isobutane, PPG-14 Butyl Ether, Fragrance (Parfum), Disteardimonium Hectorite, Propane, BHT, Propylene Carbonate.
Questions?
Call toll-free 1-800-450-7580
Packaging
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 64942-1570-1 | 2025-01-30 | C162847 | 48780-1 | 9d75b9d0-ed31-f424-e053-dadaa90a57ce | Axe Phoenix Dry Spray Antiperspirant 48HR Protection Dry |
| 64942-1570-1 | 2020-09-30 | C162847 | 48780-1 | 9d75b9d0-ed31-f424-e053-dadaa90a57ce | Axe Phoenix Dry Spray Antiperspirant 48HR Protection Dry |
| 64942-1570-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-ed31-f424-e053-dadaa90a57ce | Axe Phoenix Dry Spray Antiperspirant 48HR Protection Dry |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 64942-1570-1 | Axe | 107 g in 1 CAN | AEROSOL, SPRAY | 107 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 64942-1570 | AXE (PHOENIX DRY SPRAY ANTIPERSPIRANT 48HR PROTECTION DRY) AEROSOL, SPRAY [CONOPCO INC. D/B/A/ UNILEVER] | 3 | Legacy NDC, 1 package rows | 20211202_64516779-0352-fd0a-e053-2a91aa0a5f2f.zip |
Products#
Every source-derived product name is available through these pages.
- Axe
- Phoenix Dry Spray Antiperspirant 48HR Protection Dry
- BUTANE
- CYCLOMETHICONE 5
- 1,1-DIFLUOROETHANE
- PPG-14 BUTYL ETHER
- DISTEARDIMONIUM HECTORITE
- ALUMINUM CHLOROHYDRATE
- BUTYLATED HYDROXYTOLUENE
- PROPYLENE CARBONATE
- PROPANE
- ISOBUTANE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 64942-1570 | 64942-1570-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| BUTANE | 6LV4FOR43R | IACT |
| CYCLOMETHICONE 5 | 0THT5PCI0R | IACT |
| 1,1-DIFLUOROETHANE | 0B1U8K2ME0 | IACT |
| PPG-14 BUTYL ETHER | R199TJT95T | IACT |
| DISTEARDIMONIUM HECTORITE | X687XDK09L | IACT |
| ALUMINUM CHLOROHYDRATE | HPN8MZW13M | ACTIB |
| BUTYLATED HYDROXYTOLUENE | 1P9D0Z171K | IACT |
| PROPYLENE CARBONATE | 8D08K3S51E | IACT |
| PROPANE | T75W9911L6 | IACT |
| ISOBUTANE | BXR49TP611 | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| d217575b-5e6b-00c8-e053-2a95a90a4cae | 64516779-0352-fd0a-e053-2a91aa0a5f2f | 2021-12-01 | Warnings | d217575b-5e6b-00c8-e053-2a95a90a4cae 64516779-0352-fd0a-e053-2a91aa0a5f2f |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.