NDC11 83819060602
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 |
|---|---|
| 83819-0606-02 | 83819-0606 |
| 83819-0606-2 | 83819-0606 |
| 83819-606-02 | 83819-606 |
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 FOLLICULITIS TREATMENT | SULFUR, CURCUMA LONGA | Celcius Corp. | f43bc300-50bf-421a-81f8-1da7fc829cd0 | 2026-05-29 | Warnings | 83819-606-02 83819-606 83819060602 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.