NDC11 54622048601
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 |
|---|---|
| 54622-0486-01 | 54622-0486 |
| 54622-0486-1 | 54622-0486 |
| 54622-486-01 | 54622-486 |
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 |
|---|---|---|---|---|---|---|
| enMotion Foam High Frequency Use | ETHYL ALCOHOL | Georgia-Pacific Consumer Products LP | e56f5a94-0be1-487b-ad95-c1fe74c824ee | 2026-02-04 | Warnings, Adverse reactions | 54622-486-01 54622-486 54622048601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.