warnings
Warnings If pregnant or breast-feeding, consult a health professional before use. In case of accidental overdose, seek professional assistance or contact a poison control center immediately.
Lymphonest
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
- Lymphonest
- Generic name
- ECHINACEA AUGUSTIFOLIA, SCROPHULARIA NODOSA, ABROTANUM, PETROLEUM, ALOE SOCOTRINA, MERCURIUS SOLUBILIS, CROTALUS HORIIDUS, THUJA OCCIDENTALIS, LACHESIS MUTUS, ARISTOLOCHIA CLEMATITIS
- Manufacturer
- Marco Pharma International LLC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 84e18e97-4892-4699-b0c6-c194dc783b2d
- SPL ID
- 483c2be0-953e-7ce6-e063-6394a90a3fcd
- Version
- 6
- Effective date
- 2026-01-12
- Source export date
- 2026-10-30
- 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/2026-10-30/0b630a6825fc0c8abba22d7c8fd4d069bde78bef928766047ddbb369119f337f/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:00:10
| 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 | Lymphonest | openfda.brand_name | |
| generic name | ECHINACEA AUGUSTIFOLIA, SCROPHULARIA NODOSA, ABROTANUM, PETROLEUM, ALOE SOCOTRINA, MERCURIUS SOLUBILIS, CROTALUS HORIIDUS, THUJA OCCIDENTALIS, LACHESIS MUTUS, ARISTOLOCHIA CLEMATITIS | openfda.generic_name | |
| manufacturer name | Marco Pharma International LLC. | openfda.manufacturer_name | |
| ndc | package | 60986-1004-4 | openfda.package_ndc |
| ndc | package | 60986-1004-3 | openfda.package_ndc |
| ndc | product | 60986-1004 | openfda.product_ndc |
| ndc11 | package | 60986100403 | derived:openfda.package_ndc |
| ndc11 | package | 60986100404 | derived:openfda.package_ndc |
| spl id | 483c2be0-953e-7ce6-e063-6394a90a3fcd | id | |
| spl set id | 84e18e97-4892-4699-b0c6-c194dc783b2d | set_id | |
| unii | 324Y4038G2 | openfda.unii | |
| unii | 1NT28V9397 | openfda.unii | |
| unii | ZY0NX0W00D | openfda.unii | |
| unii | VB06AV5US8 | openfda.unii | |
| unii | V5VD430YW9 | openfda.unii | |
| unii | VSW71SS07I | openfda.unii | |
| unii | QG07G580U0 | openfda.unii | |
| unii | YHA2XLJ956 | openfda.unii | |
| unii | 1C89KKC04E | openfda.unii | |
| unii | 7H443NUB2T | 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.