NDC11 82442010616
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 |
|---|---|
| 82442-0106-16 | 82442-0106 |
| 82442-106-16 | 82442-106 |
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 |
|---|---|---|---|---|---|---|
| TARGET UP AND UP ANTICAVITY | SODIUM FLUORIDE 0.05% | TARGET CORPORATION | 2992efce-1c66-df40-e063-6294a90ab3c0 | 2025-10-08 | Warnings | 82442-106-16 82442-106 82442010616 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.