NDC11 52358000201
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 |
|---|---|
| 52358-0002-01 | 52358-0002 |
| 52358-0002-1 | 52358-0002 |
| 52358-002-01 | 52358-002 |
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 |
|---|---|---|---|---|---|---|
| SUPRADERM | WHITE PETROLATUM, LANOLIN | Olen Skin Care Corporation | 4e7199bd-52c6-48e9-9c78-c84e45412faf | 2026-06-10 | Warnings | 52358-0002-1 52358-0002 52358000201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.