NDC11 75936065301
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 |
|---|---|
| 75936-0653-01 | 75936-0653 |
| 75936-0653-1 | 75936-0653 |
| 75936-653-01 | 75936-653 |
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 |
|---|---|---|---|---|---|---|
| Play Everyday Sunscreen SPF 50 with Sunflower Extract | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | Supergoop, LLC | 0428eebc-4ffb-4981-b738-2c9ecf2a6a2e | 2026-06-04 | Warnings | 75936-653-01 75936-653 75936065301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.