warnings
Keep out of reach of children. If pregnant or breastfeeding, ask a health professional before use. Stop use and ask a doctor if symptoms persist or worsen. If you have severe symptoms, consult a doctor before use.
BM VITAGENE FORTE SOLID
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
- BM VITAGENE FORTE SOLID
- Generic name
- ACID PHOS, AGNUS CASTUS, CALADIUM SEG, DAMIANA, GINSENG PANAX, SABAL SERR, SCUTELLARIA LAT, SELENIUM, YOHIMBINUM
- Manufacturer
- Total Operations Management LLC DBA:Bestmade Natural Products Micro
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 54610bfe-87bf-06ed-e063-6394a90ae1cd
- SPL ID
- 54610801-813d-0a1c-e063-6394a90a6f66
- Version
- 1
- Effective date
- 2026-06-16
- Source export date
- 2026-10-12
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:56:24
| 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 | BM VITAGENE FORTE SOLID | openfda.brand_name | |
| generic name | ACID PHOS, AGNUS CASTUS, CALADIUM SEG, DAMIANA, GINSENG PANAX, SABAL SERR, SCUTELLARIA LAT, SELENIUM, YOHIMBINUM | openfda.generic_name | |
| manufacturer name | Total Operations Management LLC DBA:Bestmade Natural Products Micro | openfda.manufacturer_name | |
| ndc | package | 82969-6108-1 | openfda.package_ndc |
| ndc | product | 82969-6108 | openfda.product_ndc |
| ndc11 | package | 82969610801 | derived:openfda.package_ndc |
| spl id | 54610801-813d-0a1c-e063-6394a90a6f66 | id | |
| spl set id | 54610bfe-87bf-06ed-e063-6394a90ae1cd | set_id | |
| unii | J7WWH9M8QS | openfda.unii | |
| unii | 8W75VCV53Q | openfda.unii | |
| unii | 01800C6E6B | openfda.unii | |
| unii | 433OSF3U8A | openfda.unii | |
| unii | 7BP4DH5PDC | openfda.unii | |
| unii | E4GA8884NN | openfda.unii | |
| unii | RQ2CFA7WWJ | openfda.unii | |
| unii | 2Y49VWD90Q | openfda.unii | |
| unii | H6241UJ22B | 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.