NDC11 51672138202
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 |
|---|---|
| 51672-1382-02 | 51672-1382 |
| 51672-1382-2 | 51672-1382 |
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 |
|---|---|---|---|---|---|---|
| Clindamycin Phosphate and Benzoyl Peroxide | CLINDAMYCIN AND BENZOYL PEROXIDE GEL | Sun Pharmaceutical Industries, Inc. | 6df9e011-3959-411d-9e28-1df097829028 | 2026-01-20 | Warnings, Adverse reactions | 51672-1382-2 51672138202 |
| Clindamycin Phosphate and Benzoyl Peroxide | CLINDAMYCIN AND BENZOYL PEROXIDE GEL | Sun Pharmaceutical Industries, Inc. | 10e10bc2-4074-4268-916b-dd2f40fb7bb3 | 2025-07-07 | Warnings, Adverse reactions | 51672-1382-2 51672138202 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.