ACTIV-CHARCOAL ANTIFUNGAL

ACTIV-CHARCOAL ANTIFUNGAL is an FDA-registered drug product whose active ingredient is TOLNAFTATE. It is labelled by HONG KONG UNORDERED TRADING CO., LIMITED taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87800-0002, application M005, label effective 20260718. It is one of 53 FDA drug label records sharing the active ingredient TOLNAFTATE. 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 TOLNAFTATE are most often described in connection with: affected area, athlete foot, drythoroughly apply, thin layer, product overthe, twice daily, morningand night, directed doctor. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

DIRECTIONSClean the affected area and drythoroughly.Apply a thin layer of the product overthe affected area twice daily (morningand night) or as directed by a doctor.Supervise children in the use of this product.For athlete's foot, pay special attentionto spaces between the toes; wear well-fitting, ventilated shoes, and changeshoes and socks at least once daily.- For athlete's foot and ringworm, usedaily for 4 weeks.For jock itch, use daily for 2 weeks.If condition persists longer, consult adoctor. This product is not effective on the scalp or nails.

For athlete's foot and ringworm, use daily for 4 weeks. For jock itch, use daily for 2 weeks. If condition persists longer, consult a doctor.

WARNINGSFor external use only.

FDA lists 53 drug label records with TOLNAFTATE 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 ACTIV-CHARCOAL ANTIFUNGAL used for?
DIRECTIONSClean the affected area and drythoroughly.Apply a thin layer of the product overthe affected area twice daily (morningand night) or as directed by a doctor.Supervise children in the use of this product.For athlete's foot, pay special attentionto spaces between the toes; wear well-fitting, ventilated shoes, and changeshoes and socks at least once daily.- For athlete's foot and ringworm, …

Who makes ACTIV-CHARCOAL ANTIFUNGAL?
HONG KONG UNORDERED TRADING CO., LIMITED is the labeler of record for ACTIV-CHARCOAL ANTIFUNGAL. 53 FDA label records share the active ingredient TOLNAFTATE, 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 ACTIV-CHARCOAL ANTIFUNGAL 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 ACTIV-CHARCOAL ANTIFUNGAL 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 TOLNAFTATE?
Yes. 53 FDA drug label records list TOLNAFTATE 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 ACTIV-CHARCOAL ANTIFUNGAL 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.