DB Foot Pain Relieving

DB Foot Pain Relieving is an FDA-registered drug product whose active ingredient is APIS MELLIFICA, GELSEMIUM SEMPERVIRENS, GNAPHALIUM. It is labelled by The Magni Company taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 43689-0070, label effective 20260526. 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 MELLIFICA, GELSEMIUM SEMPERVIRENS, GNAPHALIUM 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.

Use: Temporarily Relieves Foot Pain

Directions: - Adults and children 12 years of age and older, apply to all surfaces on the feet, heels and toes up to four times daily - Apply to legs as needed

Warnings: For external use only

What is DB Foot Pain Relieving used for?
Use: Temporarily Relieves Foot Pain

Who makes DB Foot Pain Relieving?
The Magni Company is the labeler of record for DB Foot Pain Relieving.

What form does DB Foot Pain Relieving 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 DB Foot Pain Relieving 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.

Has DB Foot Pain Relieving 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.