NDC11 80684018001
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 |
|---|---|
| 80684-0180-01 | 80684-0180 |
| 80684-0180-1 | 80684-0180 |
| 80684-180-01 | 80684-180 |
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-Pure Hand SanitizerTropical Burst Scented | ALCOHOL | Fourstar Group USA, Inc. | 67fe2f38-ed73-4fe7-9056-fa87f7300403 | 2025-12-02 | Warnings | 80684-180-01 80684-180 80684018001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.