NDC11 82442050374
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 |
|---|---|
| 82442-0503-74 | 82442-0503 |
| 82442-503-74 | 82442-503 |
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 |
|---|---|---|---|---|---|---|
| UP AND UP MUCUS RELIEF | GUAIFENESIN | Target Corporation | 059cff23-b6a5-40dc-ac4e-9bcb552e9764 | 2025-09-22 | Warnings | 82442-503-74 82442-503 82442050374 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.