NDC11 80641001787
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 |
|---|---|
| 80641-0017-87 | 80641-0017 |
| 80641-017-87 | 80641-017 |
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 |
|---|---|---|---|---|---|---|
| Vacation Super | AVOBENZONE HOMOSALATE OCTISALATE OCTOCRYLENE | Vacation Inc. | 137c350b-dca1-47f7-e063-6294a90a531e | 2024-03-12 | Warnings | 80641-017-87 80641-017 80641001787 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.