NDC11 52494010025
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 |
|---|---|
| 52494-0100-25 | 52494-0100 |
| 52494-100-25 | 52494-100 |
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 |
|---|---|---|---|---|---|---|
| Method Men Face with Zinc Oxide Sunscreen | ZINC OXIDE | Method Products Inc. | cce5f8e1-cf40-4524-af2b-1d49309e2809 | 2024-12-12 | Warnings | 52494-100-25 52494-100 52494010025 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.