NDC11 37808095612
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 |
|---|---|
| 37808-0956-12 | 37808-0956 |
| 37808-956-12 | 37808-956 |
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 |
|---|---|---|---|---|---|---|
| H.E.B Solutions Sunscreen | ULTRA SPF 50 LOTION | H.E.B | 12c76c72-4411-48d5-b79b-c58703bf1fdd | 2024-10-15 | Warnings | 37808-956-12 37808-956 37808095612 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.