NDC11 51316049709
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 |
|---|---|
| 51316-0497-09 | 51316-0497 |
| 51316-0497-9 | 51316-0497 |
| 51316-497-09 | 51316-497 |
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 |
|---|---|---|---|---|---|---|
| ALLERGY RELIEF | FLUTICASONE PROPIONATE | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 1a4f4449-a8d3-4c5b-8ba1-21223574545b | 2026-02-17 | Warnings | 51316-497-09 51316-497 51316049709 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.