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
- BLACK FROZEN PEAR AND CEDARWOOD SCENT 48H FRESH AND DRY ANTIPERSPIRANT
- Manufacturer
- Conopco Inc. d/b/a/ Unilever
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 00d63f96-10ec-668b-e063-6394a90a72c8
- SPL ID
- 26471cf8-05b6-0482-e063-6394a90aac64
- Version
- 2
- Effective date
- 2024-11-06
- Source export date
- 2026-11-06
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/97001096994db9ca8cee114e6c3bb5298d3c573158ffc1ab8692d82e76a3eb40/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 06:54:36
| 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 | BLACK FROZEN PEAR AND CEDARWOOD SCENT 48H FRESH AND DRY ANTIPERSPIRANT | openfda.generic_name | |
| manufacturer name | Conopco Inc. d/b/a/ Unilever | openfda.manufacturer_name | |
| ndc | package | 64942-2123-1 | openfda.package_ndc |
| ndc | product | 64942-2123 | openfda.product_ndc |
| ndc11 | package | 64942212301 | derived:openfda.package_ndc |
| spl id | 26471cf8-05b6-0482-e063-6394a90aac64 | id | |
| spl set id | 00d63f96-10ec-668b-e063-6394a90a72c8 | 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.