NDC11 48951111702
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 |
|---|---|
| 48951-1117-02 | 48951-1117 |
| 48951-1117-2 | 48951-1117 |
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 Betula B | ARNICA BETULA B | Uriel Pharmacy Inc. | 7ed77c5d-5a3f-4b28-acd1-7796f3b5ef8c | 2025-06-27 | Warnings | 48951-1117-2 48951-1117 48951111702 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.