Axe Urban Dry Spray Antiperspirant
- Manufacturer
- Conopco Inc. d/b/a Unilever
- Effective date
- 2018-12-12
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 22:57:37
Label at a glance#
Contacts and useful links#
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
3.8 oz PDP
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 64942-1406-1 | 2023-07-28 | C162847 | 48780-1 | 0191ceaa-644c-198a-e063-dbdaa90aec3e | Axe Urban Dry Spray Antiperspirant |
| 64942-1406-2 | 2023-07-28 | C162847 | 48780-1 | 0191ceaa-644c-198a-e063-dbdaa90aec3e | Axe Urban Dry Spray Antiperspirant |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 64942-1406-1 | AxeUrban Antiperspirant | 107 g in 1 CAN | AEROSOL, SPRAY | 107 | 2 | |
| 64942-1406-2 | AxeUrban Antiperspirant | 28 g in 1 CAN | AEROSOL, SPRAY | 28 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 64942-1406 | AXE URBAN ANTIPERSPIRANT (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [CONOPCO INC. D/B/A UNILEVER] | 2 | Legacy NDC, 2 package rows | 20181213_c1d9b992-ba7d-4349-b275-412dcc129cab.zip |
Products#
Every source-derived product name is available through these pages.
- Axe Urban Antiperspirant
- Aluminum Chlorohydrate
- BUTANE
- 1,1-DIFLUOROETHANE
- CYCLOMETHICONE 5
- ISOBUTANE
- PPG-14 BUTYL ETHER
- DISTEARDIMONIUM HECTORITE
- PROPANE
- BUTYLATED HYDROXYTOLUENE
- PROPYLENE CARBONATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 64942-1406 | 64942-1406-1, 64942-1406-2 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| BUTANE | 6LV4FOR43R | IACT |
| 1,1-DIFLUOROETHANE | 0B1U8K2ME0 | IACT |
| CYCLOMETHICONE 5 | 0THT5PCI0R | IACT |
| ISOBUTANE | BXR49TP611 | IACT |
| PPG-14 BUTYL ETHER | R199TJT95T | IACT |
| DISTEARDIMONIUM HECTORITE | X687XDK09L | IACT |
| PROPANE | T75W9911L6 | IACT |
| BUTYLATED HYDROXYTOLUENE | 1P9D0Z171K | IACT |
| PROPYLENE CARBONATE | 8D08K3S51E | IACT |
| ALUMINUM CHLOROHYDRATE | HPN8MZW13M | ACTIB |
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 |
|---|---|---|---|---|---|---|
| 7cdc4969-ac48-677a-e053-2991aa0a9906 | c1d9b992-ba7d-4349-b275-412dcc129cab | 2018-12-12 | Warnings | 7cdc4969-ac48-677a-e053-2991aa0a9906 c1d9b992-ba7d-4349-b275-412dcc129cab |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
