NDC11 59899001201
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 |
|---|---|
| 59899-0012-01 | 59899-0012 |
| 59899-0012-1 | 59899-0012 |
| 59899-012-01 | 59899-012 |
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 |
|---|---|---|---|---|---|---|
| Youth 3 Activating BB Cream SPF 30 Medium | ZINC OXIDE, TITANIUM DIOXIDE | Shaklee Corporation | ccc80ea4-f270-4fd4-970c-eaa63df936e4 | 2024-06-06 | Warnings | 59899-012-01 59899-012 59899001201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.