NDC11 72036020402
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 |
|---|---|
| 72036-0204-02 | 72036-0204 |
| 72036-0204-2 | 72036-0204 |
| 72036-204-02 | 72036-204 |
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 Maximum Strength | GUAIFENESIN | HARRIS TEETER | 114a8c26-25be-5a0b-e063-6294a90a3e18 | 2024-06-14 | Warnings | 72036-204-02 72036-204 72036020402 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.