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 BM240 DROPS
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 BM240 DROPS
- Generic name
- AGRIMONIA, ARSENIC ALBUM, HYDRASTIS CAN, KALI BICH, KREOSOTUM, GRAPHITE, CIMICIFUGA, NITRICUM ACIDUM
- Manufacturer
- Total Operations Management LLC DBA:Bestmade Natural Products Micro
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 54397bb7-1842-72a7-e063-6394a90abbd1
- SPL ID
- 54399904-c3d1-7866-e063-6394a90aef85
- Version
- 1
- Effective date
- 2026-06-14
- Source export date
- 2026-10-12
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:14:31
| 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 BM240 DROPS | openfda.brand_name | |
| generic name | AGRIMONIA, ARSENIC ALBUM, HYDRASTIS CAN, KALI BICH, KREOSOTUM, GRAPHITE, CIMICIFUGA, NITRICUM ACIDUM | openfda.generic_name | |
| manufacturer name | Total Operations Management LLC DBA:Bestmade Natural Products Micro | openfda.manufacturer_name | |
| ndc | package | 82969-2540-1 | openfda.package_ndc |
| ndc | product | 82969-2540 | openfda.product_ndc |
| ndc11 | package | 82969254001 | derived:openfda.package_ndc |
| spl id | 54399904-c3d1-7866-e063-6394a90aef85 | id | |
| spl set id | 54397bb7-1842-72a7-e063-6394a90abbd1 | set_id | |
| unii | R763EBH88T | openfda.unii | |
| unii | 4QQN74LH4O | openfda.unii | |
| unii | 411VRN1TV4 | openfda.unii | |
| unii | EBU0U94820 | openfda.unii | |
| unii | S7V92P67HO | openfda.unii | |
| unii | T4423S18FM | openfda.unii | |
| unii | 3JYG22FD73 | openfda.unii | |
| unii | K73E24S6X9 | 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.