NDC11 48951113201
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 |
|---|---|
| 48951-1132-01 | 48951-1132 |
| 48951-1132-1 | 48951-1132 |
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 |
|---|---|---|---|---|---|---|
| Arnica e pl. tota 6 | ARNICA E PL. TOTA 6 | Uriel Pharmacy Inc. | d84176b5-8e86-4055-abf5-f4a80ad4334f | 2026-02-27 | Warnings | 48951-1132-1 48951-1132 48951113201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.