NDC11 62169020312
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 |
|---|---|
| 62169-0203-12 | 62169-0203 |
| 62169-203-12 | 62169-203 |
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 |
|---|---|---|---|---|---|---|
| ANIOSGEL 85 NPC | ETHANOL | Laboratoires Anios | 5ee820cd-2dca-40d5-bd96-bbd54131c2f0 | 2025-02-11 | Warnings | 62169-203-12 62169-203 62169020312 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.