Otc - Active Ingredient
Kali Sulph 6X
Bm Kali Sulph Tablet
FDA Label NDC 82969-1107
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Total Operations Management Llc Dba:bestmade Natural Products Micro for the product Bm Kali Sulph (NDC 82969-1107). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, inactive ingredient, warnings, otc - keep out of reach of children, dosage & administration, indications & usage, otc - purpose, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Lactose, Magnesium Stearate
Warnings
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
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
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
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
Kali Sulph 6X ...... cold symptoms, congestion. skin eruptions
Package Label.Principal Display Panel
Package 1 (30g)
Package 2 (500g)
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