NDC11 52000010204
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 |
|---|---|
| 52000-0102-04 | 52000-0102 |
| 52000-0102-4 | 52000-0102 |
| 52000-102-04 | 52000-102 |
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 |
|---|---|---|---|---|---|---|
| UNIVERSAL COCOA BUTTER SCENT PETROLEUM | WHITE PETROLEUM | Universal Distribution Center LLC | cf888bf3-6950-43aa-b4be-5a32961b4d96 | 2023-11-15 | Warnings | 52000-102-04 52000-102 52000010204 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.