FDA.reportPublic FDA data

BMNP Kali Sulph 6X

Manufacturer
Total Operations Management LLC DBA:Bestmade Natural Products Micro | BM Private Limited
Effective date
2026-06-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-06-12 05:10:08

Label at a glance#

ProductBM Kali Sulph
Active ingredientPOTASSIUM SULFATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Kali Sulph 6X

INACTIVE INGREDIENT SECTION

Lactose, Magnesium Stearate

WARNINGS SECTION

Keep out of reach of children.

If pregnant or breastfeeding, ask a health professional before use.

Stop use and ask a doctor if symptoms persist or worsen.

If you have severe symptoms, consult a doctor before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If pregnant or breastfeeding, ask a health professional before use.

Stop use and ask a doctor if symptoms persist or worsen.

If you have severe symptoms, consult a doctor before use.

DOSAGE & ADMINISTRATION SECTION

Use as directed.
Take with water, 3-4 times daily. Ages 12 and older: 5 pellets. Ages 3 to 11: 3 pellets. Ages below 3: consult your doctor.

INDICATIONS & USAGE SECTION

Helps temporarily relieve: skin eruptions and scalp issues, especially those with yellow crusting or discharge; occasional cough and nasal irritation accompanied by yellow discharge.

OTC - PURPOSE SECTION

Kali Sulph 6X ...... cold symptoms, congestion. skin eruptions

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package 1 (30g)

KALI SULPH LABELKALI SULPH LABEL

KALI SULPH PILLOW BOXKALI SULPH PILLOW BOX

kali sulph cartonkali sulph carton

Package 2 (500g)

KALI SULPH JARKALI SULPH JAR

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82969-110782969-1107-1, 82969-1107-2
85816-1007

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
MAGNESIUM STEARATE70097M6I30IACT
POTASSIUM SULFATE1K573LC5TVACTIB
LACTOSEJ2B2A4N98GIACT

Source Document#

Source XML

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 · 2 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 (package): 82969-1107-2
ndc (package): 82969-1107-1
ndc (product): 82969-1107
ndc11 (package): 82969110701
ndc11 (package): 82969110702
spl id: 53bab21a-ffe6-888a-e063-6394a90acfba
spl set id: 53bab25f-a4bf-83dd-e063-6394a90a6f0a
BM Kali SulphKALI SULPHURICUMBM Private Limited37b15ecc-7417-17c3-e063-6294a90a29082025-12-02WarningsExact identifier
ndc (product): 85816-1007

Reported adverse events (FAERS/openFDA)#

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