NDC11 69630000401
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 |
|---|---|
| 69630-0004-01 | 69630-0004 |
| 69630-0004-1 | 69630-0004 |
| 69630-004-01 | 69630-004 |
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 |
|---|---|---|---|---|---|---|
| Zinc Oxide 20% | SUNSCREEN SPF 50 | The Soleil Group, LLC | 27d20573-0b6b-4d4b-94ca-69b476a883a7 | 2026-03-23 | Warnings | 69630-004-01 69630-004 69630000401 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.