NDC11 16714072902
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 |
|---|---|
| 16714-0729-02 | 16714-0729 |
| 16714-0729-2 | 16714-0729 |
| 16714-729-02 | 16714-729 |
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 |
|---|---|---|---|---|---|---|
| Desonide | DESONIDE | NORTHSTAR RX LLC | 0665dd04-1d0b-45bf-90e4-c6e0bd90956d | 2023-07-19 | Adverse reactions | 16714-729-02 16714-729 16714072902 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.