NDC11 11673081347
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 |
|---|---|
| 11673-0813-47 | 11673-0813 |
| 11673-813-47 | 11673-813 |
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 strength antacid Peppermint Flavored | CALCIIUM CARBONATE | Target Corporation | 55dc1614-8fc0-4f2c-abfc-b675173b4f07 | 2025-11-04 | Warnings | 11673-813-47 11673-813 11673081347 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.