NDC11 57619030303
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 |
|---|---|
| 57619-0303-03 | 57619-0303 |
| 57619-0303-3 | 57619-0303 |
| 57619-303-03 | 57619-303 |
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 |
|---|---|---|---|---|---|---|
| Splash Tears | HYPROMELLOSE | LABORATORIOS SOPHIA, S.A. DE C.V. | a58a8478-9cc5-aa39-e053-2995a90a347d | 2026-05-08 | Warnings | 57619-303-03 57619-303 57619030303 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.