NDC11 11673053902
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 |
|---|---|
| 11673-0539-02 | 11673-0539 |
| 11673-0539-2 | 11673-0539 |
| 11673-539-02 | 11673-539 |
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 |
|---|---|---|---|---|---|---|
| Guaifenesin | GUAIFENESIN | TARGET CORPORATION | 0a0aa190-8dc7-f9cc-e063-6394a90a6078 | 2025-12-19 | Warnings | 11673-539-02 11673-539 11673053902 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.