United States · FDA National Drug Code directory
BM BM38 DROPS
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 82969-2338_5410afaa-6b81-f7e1-e063-6294a90a8706
- Product NDC
- 82969-2338
- Form
- LIQUID
- Composition / generic term
- Berb Aqui, Graphite, Hydrocotyle, Kali Brom, Kali Iodat, Natrum Phos, Sulphur Iodat
- Labeler
- Total Operations Management LLC DBA:Bestmade Natural Products Micro
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20150101
- Source listing expiry
- 20271231
Source-listed ingredients
- SULFUR IODIDE — 7 [hp_X]/mL
- POTASSIUM IODIDE — 7 [hp_X]/mL
- POTASSIUM BROMIDE — 7 [hp_X]/mL
- GRAPHITE — 18 [hp_X]/mL
- SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE — 12 [hp_X]/mL
- BERBERIS AQUIFOLIUM ROOT BARK — 2 [hp_X]/mL
- CENTELLA ASIATICA WHOLE — 2 [hp_X]/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 30 mL in 1 BOTTLE, GLASS (82969-2338-1) · 82969-2338-1
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →