NDC11 59735092202
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 |
|---|---|
| 59735-0922-02 | 59735-0922 |
| 59735-0922-2 | 59735-0922 |
| 59735-922-02 | 59735-922 |
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 |
|---|---|---|---|---|---|---|
| Naturium Dew Glow Tinted Moisturizer SPF50-medium | HOMOSALATE, OCTISALATE, AVOBENZONE | PML NYC, LLC | 1c3489a6-5b98-2dc2-e063-6294a90a0695 | 2026-04-14 | Warnings | 59735-922-02 59735-922 59735092202 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.