NDC11 51672135708
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 |
|---|---|
| 51672-1357-08 | 51672-1357 |
| 51672-1357-8 | 51672-1357 |
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 |
|---|---|---|---|---|---|---|
| Fluocinolone Acetonide | FLUOCINOLONE ACETONIDE | Sun Pharmaceutical Industries, Inc. | b6796a10-9c90-429d-bfd6-33b557dc952c | 2025-09-02 | Warnings, Adverse reactions | 51672-1357-8 51672-1357 51672135708 |