NDC11 70797031901
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 |
|---|---|
| 70797-0319-01 | 70797-0319 |
| 70797-0319-1 | 70797-0319 |
| 70797-319-01 | 70797-319 |
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 Infant Cough Relief | ANTIMONIUM TARTARICUM 12X,DROSERA ROTUNDIFOLIA 12X,IPECACUANHA 12X,PHOSPHORUS 12X,RUMEX CRISPUS 12X,SPONGIA TOSTA 12X,STICTA PULMONARIA 12X,KALI SULPHURICUM 6X | Talbots Pharmaceuticals Family Products, LLC. | e8902c05-3303-2e0f-e053-2a95a90aa15d | 2022-09-12 | Warnings | 70797-319-01 70797-319 70797031901 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.