QualiLife persimmon foot and shoe

QualiLife persimmon foot and shoe is an FDA-registered drug product whose active ingredient is UNDECYLENIC ACID. It is labelled by Guangdong Aimu Biological Technology Co., Ltd taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 83566-618, application M005, label effective 20260810. It is one of 24 FDA drug label records sharing the active ingredient UNDECYLENIC ACID. 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 UNDECYLENIC ACID are most often described in connection with: athlete foot, odor control, shoes eet, relieves itchy, scaly skin, toes proven, helps keep, coming back. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses For the treatment of most athlete's foot. Odor control & Deodorizer for shoes &f eet. Relieves itchy, scaly skin between the toes. Proven effective in the prevention of most athlete's foot (dermatophytosis)with daily use. Clears up most athlete's foot infection and with daily use helps keep it from coming back.

Directions Read all warnings and directions. Use only as directed. For use on feet: Wash the affected area and dry thoroughly. Spray a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor. Supervise children in the use of this product. For athlete's foot: Pay special attention to spaces between the toes;wear well-fitting, ventilated shoes, andchange shoes and socks at least once daily. For athlete's foot, use daily for 4 weeks.If condition persists longer, consult adoctor. This product is not effectiveon the scalp or nails. For use on shoes: If you have just worn your shoes,take off your shoes & allow them to sit for 15+ minutes. Shake the bottle lightly and spray 1-2 times in each shoe. Allow shoes to dry for 10+ minutes before putting back on.

Warnings For external use only

FDA lists 24 drug label records with UNDECYLENIC ACID 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 QualiLife persimmon foot and shoe used for?
Uses For the treatment of most athlete's foot. Odor control & Deodorizer for shoes &f eet. Relieves itchy, scaly skin between the toes. Proven effective in the prevention of most athlete's foot (dermatophytosis)with daily use. Clears up most athlete's foot infection and with daily use helps keep it from coming back.

Who makes QualiLife persimmon foot and shoe?
Guangdong Aimu Biological Technology Co., Ltd is the labeler of record for QualiLife persimmon foot and shoe. 24 FDA label records share the active ingredient UNDECYLENIC ACID, 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 QualiLife persimmon foot and shoe 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 QualiLife persimmon foot and shoe 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 UNDECYLENIC ACID?
Yes. 24 FDA drug label records list UNDECYLENIC ACID 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 QualiLife persimmon foot and shoe 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.