Aleve
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
- Aleve
- Generic name
- NAPROXEN SODIUM
- Manufacturer
- Bayer HealthCare LLC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 00ef5b30-71d0-4cb4-84a3-48c67d1cea2a
- SPL ID
- 4526b265-424f-3e71-e063-6294a90a21a8
- Version
- 19
- Effective date
- 2025-12-04
- Source export date
- 2026-10-30
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/57469fe40e5b1c0d9604dc7dbc22532ea48e8e53acfb911fc676578d98492f7e/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 18:29:22
| Harmonized routes |
|---|
| ORAL |
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 applno | NDA | 020204 | derived:openfda.application_number |
| application number | NDA020204 | openfda.application_number | |
| brand name | Aleve | openfda.brand_name | |
| generic name | NAPROXEN SODIUM | openfda.generic_name | |
| manufacturer name | Bayer HealthCare LLC. | openfda.manufacturer_name | |
| ndc | package | 0280-6010-02 | openfda.package_ndc |
| ndc | package | 0280-6010-01 | openfda.package_ndc |
| ndc | package | 0280-6010-50 | openfda.package_ndc |
| ndc | package | 0280-6010-05 | openfda.package_ndc |
| ndc | package | 0280-6010-06 | openfda.package_ndc |
| ndc | package | 0280-6010-04 | openfda.package_ndc |
| ndc | package | 0280-6010-10 | openfda.package_ndc |
| ndc | package | 0280-6010-24 | openfda.package_ndc |
| ndc | package | 0280-6010-03 | openfda.package_ndc |
| ndc | package | 0280-6010-09 | openfda.package_ndc |
| ndc | package | 0280-6010-07 | openfda.package_ndc |
| ndc | product | 0280-6010 | openfda.product_ndc |
| ndc11 | package | 00280601050 | derived:openfda.package_ndc |
| ndc11 | package | 00280601003 | derived:openfda.package_ndc |
| ndc11 | package | 00280601009 | derived:openfda.package_ndc |
| ndc11 | package | 00280601006 | derived:openfda.package_ndc |
| ndc11 | package | 00280601002 | derived:openfda.package_ndc |
| ndc11 | package | 00280601001 | derived:openfda.package_ndc |
| ndc11 | package | 00280601007 | derived:openfda.package_ndc |
| ndc11 | package | 00280601010 | derived:openfda.package_ndc |
| ndc11 | package | 00280601004 | derived:openfda.package_ndc |
| ndc11 | package | 00280601005 | derived:openfda.package_ndc |
| ndc11 | package | 00280601024 | derived:openfda.package_ndc |
| rxcui | 849574 | openfda.rxcui | |
| rxcui | 849728 | openfda.rxcui | |
| spl id | 4526b265-424f-3e71-e063-6294a90a21a8 | id | |
| spl set id | 00ef5b30-71d0-4cb4-84a3-48c67d1cea2a | set_id | |
| unii | 9TN87S3A3C | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.