warnings
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Polygonum
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Polygonum
- Generic name
- POLYGONUM AVICULARE, ACORUS CALAMUS, RHUS TOXICODENDRON, GNAPHALIUM POLYCEPHALUM, RHODODENDRON CHRYSANTHUM, COLOCYNTHIS, COLCHICUM AUTUMNALE, KALI IODATUM, ICHTHYOLUM, SYMPHYTUM OFFICINALE
- Manufacturer
- Marco Pharma International LLC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- e1711c08-0dfc-6267-e053-2a95a90a1cd7
- SPL ID
- 483c0bdf-aa30-601e-e063-6394a90a33c8
- Version
- 3
- Effective date
- 2026-01-12
- Source export date
- 2026-09-28
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:48:04
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| brand name | Polygonum | openfda.brand_name | |
| generic name | POLYGONUM AVICULARE, ACORUS CALAMUS, RHUS TOXICODENDRON, GNAPHALIUM POLYCEPHALUM, RHODODENDRON CHRYSANTHUM, COLOCYNTHIS, COLCHICUM AUTUMNALE, KALI IODATUM, ICHTHYOLUM, SYMPHYTUM OFFICINALE | openfda.generic_name | |
| manufacturer name | Marco Pharma International LLC. | openfda.manufacturer_name | |
| ndc | package | 60986-1032-4 | openfda.package_ndc |
| ndc | package | 60986-1032-3 | openfda.package_ndc |
| ndc | product | 60986-1032 | openfda.product_ndc |
| ndc11 | package | 60986103203 | derived:openfda.package_ndc |
| ndc11 | package | 60986103204 | derived:openfda.package_ndc |
| spl id | 483c0bdf-aa30-601e-e063-6394a90a33c8 | id | |
| spl set id | e1711c08-0dfc-6267-e053-2a95a90a1cd7 | set_id | |
| unii | 993QHL78E6 | openfda.unii | |
| unii | NQ14646378 | openfda.unii | |
| unii | M9VVZ08EKQ | openfda.unii | |
| unii | 6IO182RP7A | openfda.unii | |
| unii | IV92NQJ73U | openfda.unii | |
| unii | Q46A6NDR5C | openfda.unii | |
| unii | 36XQ854NWW | openfda.unii | |
| unii | 1C4QK22F9J | openfda.unii | |
| unii | ZCD6009IUF | openfda.unii | |
| unii | 23H32AOH17 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.