NDC11 71971907708
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 |
|---|---|
| 71971-9077-08 | 71971-9077 |
| 71971-9077-8 | 71971-9077 |
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 |
|---|---|---|---|---|---|---|
| Kids Relief | PULSATILLA, ALLIUM CEPA, ARSENICUM ALBUM, NUX VOMICA, EUPHRASIA OFFINALIS, SABADILLA, STICTA PULMONARIA, ARAILA RACEMOSA, CUPRUM METALLICUM | Homeolab International (Canada) inc | ba120c26-1e84-48b9-b38a-df5aa75ea6ce | 2019-07-16 | Warnings | 71971-9077-8 71971-9077 71971907708 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.