NDC11 46123000606
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 |
|---|---|
| 46123-0006-06 | 46123-0006 |
| 46123-0006-6 | 46123-0006 |
| 46123-006-06 | 46123-006 |
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 |
|---|---|---|---|---|---|---|
| Nitrous Oxide | NITROUS OXIDE | Roberts Oxygen Company, Inc. | 988190eb-1449-482c-8120-c1d1390e2442 | 2025-11-17 | 46123-006-06 46123-006 46123000606 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.