NDC11 52000022001
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 |
|---|---|
| 52000-0220-01 | 52000-0220 |
| 52000-0220-1 | 52000-0220 |
| 52000-220-01 | 52000-220 |
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 |
|---|---|---|---|---|---|---|
| Ice Gel ICE COLD ANALGESIC | MENTHOL | Universal Distribution Center LLC | 4f921ced-7722-cba5-e063-6294a90a650b | 2026-04-16 | Warnings | 52000-220-01 52000-220 52000022001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.