warnings
Warnings: Stop use if symptoms persist or worsen. If you are pregnant or breastfeeding, consult a health care professional prior to use. Keep out of reach of children.
Anxiovita
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
- Anxiovita
- Generic name
- ACONITUM NAPELLUS, ANACARDIUM ORIENTALE, CEREBRUM, HYPERICUM PERFORATUM
- Manufacturer
- RUBIMED AG
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 258c677b-1a0a-4315-ba0c-4d9892f0534d
- SPL ID
- 2816f87f-0405-eba7-e063-6394a90ab393
- Version
- 2
- Effective date
- 2024-10-29
- Source export date
- 2026-09-28
- Source partition
- 14
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:40:55
| 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 | Anxiovita | openfda.brand_name | |
| generic name | ACONITUM NAPELLUS, ANACARDIUM ORIENTALE, CEREBRUM, HYPERICUM PERFORATUM | openfda.generic_name | |
| manufacturer name | RUBIMED AG | openfda.manufacturer_name | |
| ndc | package | 66343-082-60 | openfda.package_ndc |
| ndc | product | 66343-082 | openfda.product_ndc |
| ndc11 | package | 66343008260 | derived:openfda.package_ndc |
| spl id | 2816f87f-0405-eba7-e063-6394a90ab393 | id | |
| spl set id | 258c677b-1a0a-4315-ba0c-4d9892f0534d | set_id | |
| unii | 4GB5DQR532 | openfda.unii | |
| unii | XK4IUX8MNB | openfda.unii | |
| unii | U0NQ8555JD | openfda.unii | |
| unii | Y0F0BU8RDU | 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.