NDC11 83818002501
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 |
|---|---|
| 83818-0025-01 | 83818-0025 |
| 83818-0025-1 | 83818-0025 |
| 83818-025-01 | 83818-025 |
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 |
|---|---|---|---|---|---|---|
| SupreH Arnica Bruise Cream | SUPREH ARNICA REMEDY PLUS BRUISE CREAM | Shenzhen Xinxin Yunhai Technology Co., Ltd. | 3e41fc0e-54c3-2622-e063-6294a90a13c9 | 2025-09-07 | Warnings | 83818-025-01 83818-025 83818002501 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.