NDC11 55681004210
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 |
|---|---|
| 55681-0042-10 | 55681-0042 |
| 55681-042-10 | 55681-042 |
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 |
|---|---|---|---|---|---|---|
| ProCure Foaming Antimicrobial Hand | HAND SOAP (BENZALKONIUM CHLORIDE 0.13%) | Twin Med LLC | 3e002cee-6102-1db4-e063-6394a90ac7a1 | 2025-09-04 | Warnings | 55681-042-10 55681-042 55681004210 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.