NDC11 43689006302
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 |
|---|---|
| 43689-0063-02 | 43689-0063 |
| 43689-0063-2 | 43689-0063 |
| 43689-063-02 | 43689-063 |
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 |
|---|---|---|---|---|---|---|
| Magnilife Pain Relieving Foot | APIS MELLIFERA, LEONTOPODIUM NIVALE SUBSP. ALPINUM WHOLE, SULFUR | The Magni Group, Inc. | 626e52cc-3031-47a4-8e31-f5ae51b51846 | 2026-07-01 | Warnings | 43689-0063-2 43689-0063 43689006302 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.