NDC11 84035001350
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 |
|---|---|
| 84035-0013-50 | 84035-0013 |
| 84035-013-50 | 84035-013 |
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 |
|---|---|---|---|---|---|---|
| Dentalclean Advanced Pro | SODIUM FLUORIDE 0.24% | Rabbit Indstria e Comrcio de Produtos de Higiene Pessoal Ltda | 4d261dc8-b065-567f-e063-6294a90aa93f | 2026-09-04 | Warnings | 84035-013-50 84035-013 84035001350 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.