Magnilife DB Pain Relieving Foot

Magnilife DB Pain Relieving Foot is an FDA-registered drug product whose active ingredient is APIS MELLIFERA, LEONTOPODIUM NIVALE SUBSP. ALPINUM WHOLE, SULFUR. It is labelled by The Magni Group, Inc. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 43689-0062, label effective 20260701. It is one of 2 FDA drug label records sharing the active ingredient APIS MELLIFERA, LEONTOPODIUM NIVALE SUBSP. ALPINUM WHOLE, SULFUR. 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 APIS MELLIFERA, LEONTOPODIUM NIVALE SUBSP. ALPINUM WHOLE, SULFUR are most often described in connection with: temporarily relieves, foot pain. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses Temporarily relieves foot pain

Directions • Generously apply and massage into all surfaces of the feet, heels, and toes twice daily • Apply to legs as needed

Warnings • For external use only • Avoid contact with eyes Keep out of reach of children • If symptoms persist for more than 7 days or worsen, consult your physician Do not use on open wounds cuts, damaged, or infected skin

FDA lists 2 drug label records with APIS MELLIFERA, LEONTOPODIUM NIVALE SUBSP. ALPINUM WHOLE, SULFUR 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 Magnilife DB Pain Relieving Foot used for?
Uses Temporarily relieves foot pain

Who makes Magnilife DB Pain Relieving Foot?
The Magni Group, Inc. is the labeler of record for Magnilife DB Pain Relieving Foot. 2 FDA label records share the active ingredient APIS MELLIFERA, LEONTOPODIUM NIVALE SUBSP. ALPINUM WHOLE, SULFUR, 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 Magnilife DB Pain Relieving Foot come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Magnilife DB Pain Relieving Foot 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 APIS MELLIFERA, LEONTOPODIUM NIVALE SUBSP. ALPINUM WHOLE, SULFUR?
Yes. 2 FDA drug label records list APIS MELLIFERA, LEONTOPODIUM NIVALE SUBSP. ALPINUM WHOLE, SULFUR 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 Magnilife DB Pain Relieving Foot 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.