NDC11 85212001301
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 |
|---|---|
| 85212-0013-01 | 85212-0013 |
| 85212-0013-1 | 85212-0013 |
| 85212-013-01 | 85212-013 |
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 |
|---|---|---|---|---|---|---|
| NOAVIA PORE FIRMING SERUM | FIELD MUSHROOM,HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF WATER | Beijing JUNGE Technology Co., Ltd. | 2f06ddef-a6ac-c5bc-e063-6394a90af451 | 2025-02-26 | Warnings | 85212-0013-1 85212-0013 85212001301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.