BM Kali Sulph

BM Kali Sulph is an FDA-registered drug product whose active ingredient is KALI SULPHURICUM. It is labelled by Total Operations Management LLC DBA:Bestmade Natural Products Micro taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 82969-1107, label effective 20260608. It is one of 4 FDA drug label records sharing the active ingredient KALI SULPHURICUM. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

Across FDA labelling, products containing KALI SULPHURICUM are most often described in connection with: helps temporarily, relieve skin, scalp issues, yellow crusting, discharge occasional, nasal irritation. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

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

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.

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.

FDA lists 4 drug label records with KALI SULPHURICUM as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

What is BM Kali Sulph used for?
Helps temporarily relieve: skin eruptions and scalp issues, especially those with yellow crusting or discharge; occasional cough and nasal irritation accompanied by yellow discharge.

Who makes BM Kali Sulph?
Total Operations Management LLC DBA:Bestmade Natural Products Micro is the labeler of record for BM Kali Sulph. 4 FDA label records share the active ingredient KALI SULPHURICUM, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does BM Kali Sulph come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is BM Kali Sulph prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing KALI SULPHURICUM?
Yes. 4 FDA drug label records list KALI SULPHURICUM as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has BM Kali Sulph been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.