NDC11 70797031401
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 |
|---|---|
| 70797-0314-01 | 70797-0314 |
| 70797-0314-1 | 70797-0314 |
| 70797-314-01 | 70797-314 |
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 |
|---|---|---|---|---|---|---|
| Dr. Talbots Cough Relief | ANTIMONIUM TARTARICUM, DROSERA ROTUNDIFOLIA, IPECACUANHA, PHOSPHORUS, RUMEX CRISPUS, SPONGIA TOSTA, STICTA PULMONARIA, KALI SULPHURICUM | Talbot's Pharmaceuticals Family Products, LLC. | 91d3e4d6-356b-4e7f-e053-2a95a90a5158 | 2021-10-05 | Warnings | 70797-314-01 70797-314 70797031401 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.