NDC11 48951112802
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 |
|---|---|
| 48951-1128-02 | 48951-1128 |
| 48951-1128-2 | 48951-1128 |
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 3 | ARNICA E PL. TOTA 3 | Uriel Pharmacy Inc. | fe03c36b-d9e6-4748-9d0b-edd128731051 | 2025-06-27 | Warnings | 48951-1128-2 48951-1128 48951112802 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.