NDC11 00363083214
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 |
|---|---|
| 00363-0832-14 | 00363-0832 |
| 00363-832-14 | 00363-832 |
| 0363-0832-14 | 0363-0832 |
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 Extended Release Maximum Strength | GUAIFENESIN | Walgreens | e4b27b9b-5f3b-4314-9717-54d73cf6b74e | 2025-08-28 | Warnings | 0363-0832-14 0363-0832 00363083214 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.