NDC11 73978000901
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 |
|---|---|
| 73978-0009-01 | 73978-0009 |
| 73978-0009-1 | 73978-0009 |
| 73978-009-01 | 73978-009 |
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 |
|---|---|---|---|---|---|---|
| b.tan Beach Please SPF 7 | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | Marque of Brands Americas, LLC | bdc07d83-a34f-5262-e053-2995a90acfc3 | 2025-12-16 | Warnings | 73978-009-01 73978-009 73978000901 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.