FDA.reportPublic FDA data

BM BM38 DROPS

Product NDC
82969-2338
Requested package NDC
82969-2338-1
11-digit product format
829692338
Labeler code
82969
Product ID
82969-2338_5410afaa-6b81-f7e1-e063-6294a90a8706
Type
HUMAN OTC DRUG
Nonproprietary name
Berb Aqui, Graphite, Hydrocotyle, Kali Brom, Kali Iodat, Natrum Phos, Sulphur Iodat
Dosage form
LIQUID
Route
ORAL
Labeler
Total Operations Management LLC DBA:Bestmade Natural Products Micro
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-01-01
Substance
SULFUR IODIDE; POTASSIUM IODIDE; POTASSIUM BROMIDE; GRAPHITE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; BERBERIS AQUIFOLIUM ROOT BARK; CENTELLA ASIATICA WHOLE
Active strength
7; 7; 7; 18; 12; 2; 2 [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 BM38 DROPS
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SULFUR IODIDE7 [hp_X]/mL
POTASSIUM IODIDE7 [hp_X]/mL
POTASSIUM BROMIDE7 [hp_X]/mL
GRAPHITE18 [hp_X]/mL
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE12 [hp_X]/mL
BERBERIS AQUIFOLIUM ROOT BARK2 [hp_X]/mL
CENTELLA ASIATICA WHOLE2 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 7 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
L6L8KA2AA0Internal UNII lookup
1C4QK22F9JInternal UNII lookup
OSD78555ZMInternal UNII lookup
4QQN74LH4OInternal UNII lookup
70WT22SF4BInternal UNII lookup
VZJ9F3C3SBInternal UNII lookup
7M867G6T1UInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
5410af95-519a-f0d5-e063-6294a90ac0cfAvailable 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 BM38 DROPSBERB AQUI, GRAPHITE, HYDROCOTYLE, KALI BROM, KALI IODAT, NATRUM PHOS, SULPHUR IODATTotal Operations Management LLC DBA:Bestmade Natural Products Micro5410af95-519a-f0d5-e063-6294a90ac0cf2026-06-12WarningsExact identifier
ndc (package): 82969-2338-1
ndc (product): 82969-2338
ndc11 (package): 82969233801

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
82969-2338-18296923380130 mL in 1 BOTTLE, GLASS (82969-2338-1) 30 ml2015-01-01NoNoCurrent