NDC11 70677105001
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 |
|---|---|
| 70677-1050-01 | 70677-1050 |
| 70677-1050-1 | 70677-1050 |
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 DM | GUAIFENESIN, DEXTROMETHORPHAN HBR | Strategic Sourcing Services LLC | af359aca-ec58-47cb-843a-2def1a09a09a | 2023-04-10 | Warnings | 70677-1050-1 70677-1050 70677105001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.