NDC11 83591062900
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 83591-0629-0 | 83591-0629 |
| 83591-0629-00 | 83591-0629 |
| 83591-629-00 | 83591-629 |
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 |
|---|---|---|---|---|---|---|
| BLUESPRING Doctors Pain Formula Pain Relief | MENTHOL | ACA MANAGEMENT LLC | 98f3f719-792f-4a93-95b1-90072e0f8bf4 | 2025-07-14 | Warnings | 83591-629-00 83591-629 83591062900 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.