NDC11 70069059101
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 |
|---|---|
| 70069-0591-01 | 70069-0591 |
| 70069-0591-1 | 70069-0591 |
| 70069-591-01 | 70069-591 |
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 |
|---|---|---|---|---|---|---|
| Phenylephrine Hydrochloride | PHENYLEPHRINE HYDROCHLORIDE | Somerset Therapeutics, LLC | 170e63f1-23f4-4839-ab89-b81832d94a56 | 2025-03-05 | Warnings, Adverse reactions | 70069-591-01 70069-591 70069059101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.