NDC11 76138011206
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 |
|---|---|
| 76138-0112-06 | 76138-0112 |
| 76138-0112-6 | 76138-0112 |
| 76138-112-06 | 76138-112 |
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 |
|---|---|---|---|---|---|---|
| Antibacterial Hand Sanitizer | ETHYL ALCOHOL | Innovation Specialties Inc | 9bef34b7-fdd0-41ee-a140-ea82552aab47 | 2024-07-10 | Warnings | 76138-112 |
| Antibacterial Hand Sanitizer | ETHYL ALCOHOL | Innovation Specialties Inc | 7824f5c7-3650-490f-92cd-46c8ec32d7be | 2024-07-10 | Warnings | 76138-112-06 76138-112 76138011206 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.