NDC11 76354012001
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 |
|---|---|
| 76354-0120-01 | 76354-0120 |
| 76354-0120-1 | 76354-0120 |
| 76354-120-01 | 76354-120 |
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 |
|---|---|---|---|---|---|---|
| Naturium Sulfur Spot Treatment 8% | SULFUR | e.l.f. Cosmetics, Inc | 0a4a9aed-5eeb-f648-e063-6394a90a1d76 | 2025-11-14 | Warnings | 76354-120-01 76354-120 76354012001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.