NDC11 21749011342
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 |
|---|---|
| 21749-0113-42 | 21749-0113 |
| 21749-113-42 | 21749-113 |
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 |
|---|---|---|---|---|---|---|
| PURELL HEALTHY SP BAK E2 Antimicrobial Foam Sp | BENZALKONIUM CHLORIDE | GOJO Industries, Inc. | 4ea02d8a-cb03-4e9e-b63d-72b83fa816f8 | 2024-12-03 | Warnings | 21749-113-42 21749-113 21749011342 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.