warnings
Warnings If pregnant or breast-feeding, consult a health professional before use.
ECHINACEA
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
- ECHINACEA
- Generic name
- ECHINACEA ANGUSTIFOLIA, HAMAMMELIS VIRGINIANA, CALCAREA PHOSPHORICA, HYDRASTIS CANADANESIS, SENEGA OFFICINALIS, SILICEA, CONIUM, AURUM MURIATICUM NATRONATUM, CALCAREA CARBONICA, FUCUS VESICULOSUS, LACHESIS MUTUS
- Manufacturer
- Marco Pharma International LLC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 7efadb70-99e4-428b-a8ef-a2797327c6fa
- SPL ID
- 483b5b77-9991-87fa-e063-6394a90a6c1e
- Version
- 7
- Effective date
- 2026-01-12
- Source export date
- 2026-10-12
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:28:10
| 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 | ECHINACEA | openfda.brand_name | |
| generic name | ECHINACEA ANGUSTIFOLIA, HAMAMMELIS VIRGINIANA, CALCAREA PHOSPHORICA, HYDRASTIS CANADANESIS, SENEGA OFFICINALIS, SILICEA, CONIUM, AURUM MURIATICUM NATRONATUM, CALCAREA CARBONICA, FUCUS VESICULOSUS, LACHESIS MUTUS | openfda.generic_name | |
| manufacturer name | Marco Pharma International LLC. | openfda.manufacturer_name | |
| ndc | package | 60986-2020-2 | openfda.package_ndc |
| ndc | product | 60986-2020 | openfda.product_ndc |
| ndc11 | package | 60986202002 | derived:openfda.package_ndc |
| spl id | 483b5b77-9991-87fa-e063-6394a90a6c1e | id | |
| spl set id | 7efadb70-99e4-428b-a8ef-a2797327c6fa | set_id | |
| unii | Q28R5GF371 | openfda.unii | |
| unii | 91D9GV0Z28 | openfda.unii | |
| unii | ETJ7Z6XBU4 | openfda.unii | |
| unii | 2E32821G6I | openfda.unii | |
| unii | VB06AV5US8 | openfda.unii | |
| unii | 535G2ABX9M | openfda.unii | |
| unii | ZW3Z11D0JV | openfda.unii | |
| unii | M7T6H7D4IF | openfda.unii | |
| unii | VSW71SS07I | openfda.unii | |
| unii | 7FT6QUT299 | openfda.unii | |
| unii | T7S323PKJS | 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.