NDC11 37808091412
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 |
|---|---|
| 37808-0914-12 | 37808-0914 |
| 37808-914-12 | 37808-914 |
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 ULTRA | SPF 50 SUNSCREEN | H.E.B | d6184ba2-0e47-459a-8777-1f27be2140a6 | 2024-10-15 | Warnings | 37808-914-12 37808-914 37808091412 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.