Home NDC 82969-1207 BMNP Kali Sulph
Product NDC 82969-1207
11-digit product format 829691207
Labeler code 82969
Product ID 82969-1207_5a54d491-5f55-0666-e063-6294a90ad138
Type HUMAN OTC DRUG
Nonproprietary name Kalium Sulphuricum
Dosage form GLOBULE
Route ORAL
Labeler Total Operations Management LLC DBA:Bestmade Natural Products Micro
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2026-06-01
Substance POTASSIUM SULFATE
Active strength 6 [hp_X]/g
Pharmacologic classes Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
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 BMNP Kali Sulph
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM SULFATE 6 [hp_X]/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1K573LC5TV Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 82969-1207-1 82969120701 25 g in 1 BOTTLE, GLASS (82969-1207-1) 25 g 2026-06-01 No No Current 82969-1207-2 82969120702 8 g in 1 BOTTLE, GLASS (82969-1207-2) 8 g 2026-06-01 No No Current