NDC11 37000061721
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 |
|---|---|
| 37000-0617-21 | 37000-0617 |
| 37000-617-21 | 37000-617 |
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 |
|---|---|---|---|---|---|---|
| Dawn Ultra Antibacterial Hand Orange Scent | CHLOROXYLENOL | The Procter & Gamble Manufacturing Company | b440e526-83c2-45b7-9c45-f95151216000 | 2026-04-01 | Warnings | 37000-617-21 37000-617 37000061721 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.