NDC11 58933004542
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 |
|---|---|
| 58933-0045-42 | 58933-0045 |
| 58933-045-42 | 58933-045 |
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 Strawberry | SODIUM FLUORIDE | Procter & Gamble Manufactura, S. de R.L. de C.V. | 01f69824-e886-6e7b-e063-6294a90acf77 | 2026-01-08 | Warnings | 58933-045-42 58933-045 58933004542 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.