NDC11 51316047002
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 |
|---|---|
| 51316-0470-02 | 51316-0470 |
| 51316-0470-2 | 51316-0470 |
| 51316-470-02 | 51316-470 |
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 |
|---|---|---|---|---|---|---|
| MUCUS RELIEF | GUAIFENESIN | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 2caa7f8e-695c-441a-a968-fcc3f527d117 | 2026-05-13 | Warnings | 51316-470-02 51316-470 51316047002 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.