NDC11 69949002501
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 |
|---|---|
| 69949-0025-01 | 69949-0025 |
| 69949-0025-1 | 69949-0025 |
| 69949-025-01 | 69949-025 |
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 |
|---|---|---|---|---|---|---|
| Mineral Sun Drops | ZINC OXIDE | Synchronicity Spa, Inc. DBA Suntegrity | d8acda81-4430-42f8-be56-d28bb010e630 | 2025-10-22 | Warnings | 69949-025-01 69949-025 69949002501 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.