NDC11 83819090002
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 |
|---|---|
| 83819-0900-02 | 83819-0900 |
| 83819-0900-2 | 83819-0900 |
| 83819-900-02 | 83819-900 |
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 COLD SORE RELIEF | CARDIOSPERMUM, CURCUMA LONGA | Celcius Corp. | d495e37e-0245-442a-8546-9f26bf1dd045 | 2026-02-09 | Warnings | 83819-900-02 83819-900 83819090002 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.