NDC11 84345008601
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 |
|---|---|
| 84345-0086-01 | 84345-0086 |
| 84345-0086-1 | 84345-0086 |
| 84345-086-01 | 84345-086 |
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 |
|---|---|---|---|---|---|---|
| CAREKON ANTI-CAVITY FLUORIDE | SODIUM MONOFLUOROPHOSPHATE | Hunan Yinhuatang Pharmaceutical Technology Co., Ltd. | 3baca3b6-ff48-0579-e063-6394a90abd08 | 2025-08-29 | Warnings | 84345-086-01 84345-086 84345008601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.