NDC11 37835099601
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 |
|---|---|
| 37835-0996-01 | 37835-0996 |
| 37835-0996-1 | 37835-0996 |
| 37835-996-01 | 37835-996 |
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 |
|---|---|---|---|---|---|---|
| Oxymetazoline Hydrochloride | OXYMETAZOLINE HYDROCHLORIDE | Bi-Mart | 4ceb21f4-e391-4a6f-8d4b-f434ed4e50bf | 2025-08-01 | Warnings | 37835-996-01 37835-996 37835099601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.