NDC11 58657012012
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 |
|---|---|
| 58657-0120-12 | 58657-0120 |
| 58657-120-12 | 58657-120 |
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 |
|---|---|---|---|---|---|---|
| Magnesium Oxide | MAGNESIUM OXIDE | Method Pharmaceuticals, LLC | 0af63651-f9d9-43b9-b6f0-4878466a82e6 | 2025-10-21 | Warnings | 58657-120-12 58657-120 58657012012 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.