warnings
Warnings • 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.
Axe
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Axe
- Generic name
- ESSENCE BLACK PEPPER AND CEDARWOOD SCENT 48H FRESH AND DRY ANTIPERSPIRANT
- Manufacturer
- Conopco Inc. d/b/a/ Unilever
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 00d5b4a7-90ba-7a7c-e063-6294a90a52b0
- SPL ID
- 253cedf0-2cb0-214a-e063-6394a90a5ade
- Version
- 2
- Effective date
- 2024-10-24
- Source export date
- 2026-09-28
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:32:49
| Harmonized routes |
|---|
| TOPICAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M019 | openfda.application_number | |
| brand name | Axe | openfda.brand_name | |
| generic name | ESSENCE BLACK PEPPER AND CEDARWOOD SCENT 48H FRESH AND DRY ANTIPERSPIRANT | openfda.generic_name | |
| manufacturer name | Conopco Inc. d/b/a/ Unilever | openfda.manufacturer_name | |
| ndc | package | 64942-2122-1 | openfda.package_ndc |
| ndc | product | 64942-2122 | openfda.product_ndc |
| ndc11 | package | 64942212201 | derived:openfda.package_ndc |
| spl id | 253cedf0-2cb0-214a-e063-6394a90a5ade | id | |
| spl set id | 00d5b4a7-90ba-7a7c-e063-6294a90a52b0 | set_id | |
| unii | 8O386558JE | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.