NDC11 83819098702
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 |
|---|---|
| 83819-0987-02 | 83819-0987 |
| 83819-0987-2 | 83819-0987 |
| 83819-987-02 | 83819-987 |
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 |
|---|---|---|---|---|---|---|
| dermveda ULTRA BALANITIS RELIEF | CARDIOSPERMUM, CURCUMA LONGA | Celcius Corp. | ab44b4af-f712-411e-9c2a-92fedb931ef2 | 2026-08-11 | Warnings | 83819-987-02 83819-987 83819098702 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.