warnings
Warnings: Stop use if symptoms persist or worsen. If you are pregnant or breastfeeding, consult a healthcare professional prior to use. Keep out of reach of children.
Emvita 23
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
- Emvita 23
- Generic name
- AGARICUS MUSCARIUS, CUPRUM MET, HYPOPHYSIS, RHUS TOX
- Manufacturer
- RUBIMED AG
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 010a76a8-da24-4dd1-9005-c0c2d25526f5
- SPL ID
- 28177a7c-9f4e-3d9b-e063-6394a90a1d33
- Version
- 2
- Effective date
- 2024-10-29
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:15:42
| 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 | Emvita 23 | openfda.brand_name | |
| generic name | AGARICUS MUSCARIUS, CUPRUM MET, HYPOPHYSIS, RHUS TOX | openfda.generic_name | |
| manufacturer name | RUBIMED AG | openfda.manufacturer_name | |
| ndc | package | 66343-110-60 | openfda.package_ndc |
| ndc | product | 66343-110 | openfda.product_ndc |
| ndc11 | package | 66343011060 | derived:openfda.package_ndc |
| spl id | 28177a7c-9f4e-3d9b-e063-6394a90a1d33 | id | |
| spl set id | 010a76a8-da24-4dd1-9005-c0c2d25526f5 | set_id | |
| unii | 789U1901C5 | openfda.unii | |
| unii | DIF093I037 | openfda.unii | |
| unii | L0PFEMQ1DT | openfda.unii | |
| unii | 6IO182RP7A | 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.