NDC11 59088021016
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 |
|---|---|
| 59088-0210-16 | 59088-0210 |
| 59088-210-16 | 59088-210 |
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 |
|---|---|---|---|---|---|---|
| Urea 39.5% with 2% Salicylic Acid | UREA, SALICYLIC ACID | PureTek Corporation | f7aa7b4f-3cb4-6113-e053-6394a90a4188 | 2023-03-24 | Warnings, Adverse reactions | 59088-210-16 59088-210 59088021016 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.