NDC11 84451000602
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 |
|---|---|
| 84451-0006-02 | 84451-0006 |
| 84451-0006-2 | 84451-0006 |
| 84451-006-02 | 84451-006 |
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 |
|---|---|---|---|---|---|---|
| OS-01 FACE SPF BD SPF 30 TINTED MEDIUM/DEEP | ZINC OXIDE | ONESKIN INC. | 35d57d3f-376c-2307-e063-6294a90adf51 | 2025-05-23 | Warnings | 84451-006-02 84451-006 84451000602 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.