NDC11 73071010101
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 |
|---|---|
| 73071-0101-01 | 73071-0101 |
| 73071-0101-1 | 73071-0101 |
| 73071-101-01 | 73071-101 |
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 |
|---|---|---|---|---|---|---|
| DEWYTREE URBAN SHADE HYALURONIC LIGHTWEIGHT SUNSCREEN | OCTOCRYLENE, HOMOSALATE, OCTISALATE, AVOBENZONE | DEWYTREE CO. ,LTD | 2f1ca6e0-f689-57c7-e063-6394a90a3da5 | 2025-10-21 | Warnings | 73071-101-01 73071-101 73071010101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.