NDC11 75124000201
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 |
|---|---|
| 75124-0002-01 | 75124-0002 |
| 75124-0002-1 | 75124-0002 |
| 75124-002-01 | 75124-002 |
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 |
|---|---|---|---|---|---|---|
| PURE O2 Pack-Solid | SODIUM CHLORITE | Pure O2 | a397afb9-53a7-e6d8-e053-2a95a90a54d4 | 2020-08-29 | Warnings | 75124-0002-1 75124-0002 75124000201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.