NDC11 62032014110
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 |
|---|---|
| 62032-0141-10 | 62032-0141 |
| 62032-141-10 | 62032-141 |
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 |
|---|---|---|---|---|---|---|
| nu-derm system normal-dry skin transformation | HYDROQUINONE, OCTISALATE AND ZINC OXIDE | OBAGI COSMECEUTICAL LLC | 7548658a-5371-4aed-baf8-e5dc54262223 | 2025-03-14 | Warnings, Adverse reactions | 62032-141-10 62032014110 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.