Aleve Back and Muscle Pain
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 Back and Muscle Pain
- Generic name
- NAPROXEN SODIUM
- Manufacturer
- Bayer HealthCare LLC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 6376e1b8-52c4-0519-e053-2a91aa0af35f
- SPL ID
- 4526b594-84b6-b981-e063-6294a90a1aed
- Version
- 19
- Effective date
- 2025-12-04
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:19:08
| 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 Back and Muscle Pain | openfda.brand_name | |
| generic name | NAPROXEN SODIUM | openfda.generic_name | |
| manufacturer name | Bayer HealthCare LLC. | openfda.manufacturer_name | |
| ndc | package | 0280-6092-08 | openfda.package_ndc |
| ndc | package | 0280-6092-24 | openfda.package_ndc |
| ndc | package | 0280-6092-05 | openfda.package_ndc |
| ndc | package | 0280-6092-50 | openfda.package_ndc |
| ndc | package | 0280-6092-04 | openfda.package_ndc |
| ndc | package | 0280-6092-07 | openfda.package_ndc |
| ndc | package | 0280-6092-09 | openfda.package_ndc |
| ndc | package | 0280-6092-06 | openfda.package_ndc |
| ndc | package | 0280-6092-12 | openfda.package_ndc |
| ndc | package | 0280-6092-10 | openfda.package_ndc |
| ndc | package | 0280-6092-02 | openfda.package_ndc |
| ndc | package | 0280-6092-25 | openfda.package_ndc |
| ndc | product | 0280-6092 | openfda.product_ndc |
| ndc11 | package | 00280609210 | derived:openfda.package_ndc |
| ndc11 | package | 00280609212 | derived:openfda.package_ndc |
| ndc11 | package | 00280609224 | derived:openfda.package_ndc |
| ndc11 | package | 00280609208 | derived:openfda.package_ndc |
| ndc11 | package | 00280609207 | derived:openfda.package_ndc |
| ndc11 | package | 00280609225 | derived:openfda.package_ndc |
| ndc11 | package | 00280609202 | derived:openfda.package_ndc |
| ndc11 | package | 00280609204 | derived:openfda.package_ndc |
| ndc11 | package | 00280609250 | derived:openfda.package_ndc |
| ndc11 | package | 00280609205 | derived:openfda.package_ndc |
| ndc11 | package | 00280609209 | derived:openfda.package_ndc |
| ndc11 | package | 00280609206 | derived:openfda.package_ndc |
| rxcui | 849574 | openfda.rxcui | |
| rxcui | 849728 | openfda.rxcui | |
| spl id | 4526b594-84b6-b981-e063-6294a90a1aed | id | |
| spl set id | 6376e1b8-52c4-0519-e053-2a91aa0af35f | set_id | |
| unii | 9TN87S3A3C | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.