NDC11 79903029240
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 |
|---|---|
| 79903-0292-40 | 79903-0292 |
| 79903-292-40 | 79903-292 |
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 |
|---|---|---|---|---|---|---|
| equate mucus-er | GUAIFENESIN | WALMART INC. | a2cc6dec-388a-46bd-9cbc-1ffb6fd1aea3 | 2026-07-02 | Warnings | 79903-292-40 79903-292 79903029240 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.