NDC11 10202006996
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 |
|---|---|
| 10202-0069-96 | 10202-0069 |
| 10202-069-96 | 10202-069 |
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 |
|---|---|---|---|---|---|---|
| Petroleum | WHITE PETROLATUM | 7-Select | 7e93df71-74bd-4d95-9a64-54756c7b234a | 2026-01-29 | Warnings, Adverse reactions | 10202-069-96 10202-069 10202006996 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.