NDC11 83878010111
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 |
|---|---|
| 83878-0101-11 | 83878-0101 |
| 83878-101-11 | 83878-101 |
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 |
|---|---|---|---|---|---|---|
| Ultra Prep Alcohol Prep Pads | ISOPROPYL ALCOHOL | Quality Medical Products USA, Inc. | f81a63dd-a699-459f-ab52-f63a6550b680 | 2024-07-16 | Warnings | 83878-101-11 83878-101 83878010111 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.