NDC11 52915005019
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 |
|---|---|
| 52915-0050-19 | 52915-0050 |
| 52915-050-19 | 52915-050 |
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 |
|---|---|---|---|---|---|---|
| SPF30 SUPER SENSITIVE SUNSCREEN | TITANIUM DIOXIDE | ORGANIC & SUSTAINABLE BEAUTY | d79cf2d9-4923-452a-bb44-67e059ee37ee | 2024-11-07 | Warnings | 52915-050-19 52915-050 52915005019 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.