NDC11 71856042300
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 |
|---|---|
| 71856-0423-0 | 71856-0423 |
| 71856-0423-00 | 71856-0423 |
| 71856-423-00 | 71856-423 |
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 |
|---|---|---|---|---|---|---|
| 7th MANNA PAIN RELIEF DROPS | MENTHOL, CAMPHOR (SYNTHETIC) | 7TH MANNA (USA) PTE. LTD. | 699c668c-4f54-4f18-b585-bdcebe7a2c4e | 2023-11-11 | Warnings | 71856-423-00 71856-423 71856042300 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.