FDA.reportPublic FDA data

BM BM240 DROPS

Product NDC
85816-2240
Requested package NDC
85816-2240-1
11-digit product format
858162240
Labeler code
85816
Product ID
85816-2240_540ead9f-ed33-6883-e063-6294a90af843
Type
HUMAN OTC DRUG
Nonproprietary name
Agrimonia, Arsenic album, Hydrastis can, Kali bich, Kreosotum, Graphite, Cimicifuga, Nitricum acidum
Dosage form
LIQUID
Route
ORAL
Labeler
BM Private Limited
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-01-01
Substance
NITRIC ACID; AGRIMONIA EUPATORIA WHOLE; POTASSIUM DICHROMATE; HYDRASTIS CANADENSIS WHOLE; ARSENIC TRIOXIDE; BLACK COHOSH; GRAPHITE; WOOD CREOSOTE
Active strength
7; 6; 4; 6; 10; 15; 15; 7 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
BM BM240 DROPS
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
NITRIC ACID7 [hp_X]/mL
AGRIMONIA EUPATORIA WHOLE6 [hp_X]/mL
POTASSIUM DICHROMATE4 [hp_X]/mL
HYDRASTIS CANADENSIS WHOLE6 [hp_X]/mL
ARSENIC TRIOXIDE10 [hp_X]/mL
BLACK COHOSH15 [hp_X]/mL
GRAPHITE15 [hp_X]/mL
WOOD CREOSOTE7 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 8 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
411VRN1TV4Internal UNII lookup
EBU0U94820Internal UNII lookup
T4423S18FMInternal UNII lookup
R763EBH88TInternal UNII lookup
S7V92P67HOInternal UNII lookup
K73E24S6X9Internal UNII lookup
4QQN74LH4OInternal UNII lookup
3JYG22FD73Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
540ead91-b415-6032-e063-6394a90aea13Available on FDA.report

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
BM BM240 DROPSAGRIMONIA, ARSENIC ALBUM, HYDRASTIS CAN, KALI BICH, KREOSOTUM, GRAPHITE, CIMICIFUGA, NITRICUM ACIDUMBM Private Limited540ead91-b415-6032-e063-6394a90aea132026-06-12WarningsExact identifier
ndc (package): 85816-2240-1
ndc (product): 85816-2240
ndc11 (package): 85816224001

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85816-2240-18581622400130 mL in 1 BOTTLE, GLASS (85816-2240-1) 30 ml2015-01-01NoNoCurrent