NDC11 58933004742
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 |
|---|---|
| 58933-0047-42 | 58933-0047 |
| 58933-047-42 | 58933-047 |
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 |
|---|---|---|---|---|---|---|
| Crest Bubblegum | SODIUM FLUORIDE | Procter & Gamble Manufacturing Mxico, S. de R.L. de C.V. | 01f618d7-be07-18c3-e063-6294a90a2d97 | 2026-01-08 | Warnings | 58933-047-42 58933-047 58933004742 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.