NDC11 69494030230
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 |
|---|---|
| 69494-0302-30 | 69494-0302 |
| 69494-302-30 | 69494-302 |
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 |
|---|---|---|---|---|---|---|
| Eryfotona Actinica Ultralight Emulsion | SUNSCREEN | ISDIN Corp | 1d4b88d3-bee9-102c-e054-00144ff8d46c | 2024-11-18 | Warnings | 69494-302-30 69494-302 69494030230 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.