ProBliva Antifungal Scrub .soap. Bar

ProBliva Antifungal Scrub .soap. Bar is an FDA-registered drug product whose active ingredient is TOLNAFTATE 1%. It is labelled by CAVTECH HOLDING LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85464-007, application M005, label effective 20260428. It is one of 39 FDA drug label records sharing the active ingredient TOLNAFTATE 1%. 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 1% are most often described in connection with: affected area, let product, sit minutes, rinsing make, sure dry, thoroughly supervise, athlete foot, pay special. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Wash affected area well and let product sit 2-3minutes before rinsing Make sure to dry affected area thoroughly Supervise children in the use of this product For Athlete's foot: pay special attention to the spacesbetween the toes; wear well-fitting, ventilated shoes and change shoes and socks at least once daily Use 1-2 times daily. Use daily for 4 weeks; if the condition persists longer, aska doctor This product is not effective on the scalp or nails.

For effective treatment of most athlete's foot(tinea pedis), ringworm(tinea corporis) and jock itch(tinea cruris) For effective relief of itching, burning and cracking skin.

For external use only When using this product Avoid contact with the eyes. Ifcontact occurs, rinse thoroughly with water. Stop and ask a doctor if Irritation occurs or if there is noimprovement within 2 weeks for jock itch or within 4 weeks for athlete's foot and ringworm Excessive irritation occurs. Do not use on broken, irritated, or severely damaged skin on children under 2 of age except under the advice and supervision of a doctor. If swallowed, get medical helpor contact a Poison Control Center right away.

FDA lists 39 drug label records with TOLNAFTATE 1% 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 ProBliva Antifungal Scrub .soap. Bar used for?
Wash affected area well and let product sit 2-3minutes before rinsing Make sure to dry affected area thoroughly Supervise children in the use of this product For Athlete's foot: pay special attention to the spacesbetween the toes; wear well-fitting, ventilated shoes and change shoes and socks at least once daily Use 1-2 times daily. Use daily for 4 weeks; if the condition persists longer, aska …

Who makes ProBliva Antifungal Scrub .soap. Bar?
CAVTECH HOLDING LLC is the labeler of record for ProBliva Antifungal Scrub .soap. Bar. 39 FDA label records share the active ingredient TOLNAFTATE 1%, 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 ProBliva Antifungal Scrub .soap. Bar 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 ProBliva Antifungal Scrub .soap. Bar 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 1%?
Yes. 39 FDA drug label records list TOLNAFTATE 1% 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 ProBliva Antifungal Scrub .soap. Bar 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.