NDC11 85163001701
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 |
|---|---|
| 85163-0017-01 | 85163-0017 |
| 85163-0017-1 | 85163-0017 |
| 85163-017-01 | 85163-017 |
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 |
|---|---|---|---|---|---|---|
| OUHOE Face Body Sunscreen | TITANIUM DIOXIDE | Shantou Ouhoe Technology Co., Ltd. | 46d36f60-2a5d-816e-e063-6294a90a2ddc | 2025-12-26 | Warnings | 85163-017-01 85163-017 85163001701 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.