BM Kali Sulph

Product NDC
82969-1107
11-digit product format
829691107
Labeler code
82969
Product ID
82969-1107_53bab21a-ffe6-888a-e063-6394a90acfba
Type
HUMAN OTC DRUG
Nonproprietary name
Kali Sulphuricum
Dosage form
TABLET
Route
ORAL
Labeler
Total Operations Management LLC DBA:Bestmade Natural Products Micro
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-01-01
Substance
POTASSIUM SULFATE
Active strength
6 [hp_X]/60mg
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
BM Kali Sulph
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
POTASSIUM SULFATE6 [hp_X]/60mg

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1K573LC5TVInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
53bab25f-a4bf-83dd-e063-6394a90a6f0aAvailable 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 Kali SulphKALI SULPHURICUMTotal Operations Management LLC DBA:Bestmade Natural Products Micro53bab25f-a4bf-83dd-e063-6394a90a6f0a2026-06-08WarningsExact identifier
ndc (product): 82969-1107

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
82969-1107-18296911070130000 mg in 1 BOTTLE, GLASS (82969-1107-1) 30000 mg2015-01-01NoNoCurrent
82969-1107-282969110702500000 mg in 1 JAR (82969-1107-2) 500000 mg2015-01-01NoNoCurrent