NDC11 49035095665
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 |
|---|---|
| 49035-0956-65 | 49035-0956 |
| 49035-956-65 | 49035-956 |
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 |
|---|---|---|---|---|---|---|
| Maximum Strength Mucus Relief DM | GUAIFENESIN AND DEXTROMETHORPHAN HBR | Wal-Mart Stores, Inc. | ff7280e7-804b-423d-add8-54ec2c76fca2 | 2026-08-28 | Warnings | 49035-956-65 49035-956 49035095665 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.