RoyceDerm Antifungal .spray.

RoyceDerm Antifungal .spray. is an FDA-registered drug product whose active ingredient is CLOTRIMAZOLE 1%. It is labelled by RoyceDerm LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85424-026, application M005, label effective 20260622. It is one of 7 FDA drug label records sharing the active ingredient CLOTRIMAZOLE 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 CLOTRIMAZOLE 1% are most often described in connection with: affected area, athlete foot, dry thoroughly, apply thin, twice daily, night directed, doctor supervise, ofthis product. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

clean the affected area and dry thoroughly. apply 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 ofthis product. for athlete's foot: pay special attention to the spaces between the toes; wear well-fitting,ventilated shoes and change shoes & socks at least once daily. 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. this product is not effective on the scalp or nails.

For effective treatment of most athlete's foot(tineapedis), 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 eye Stop and ask a doctor if irritation occurs or if there is no improvement within 2 weeks for jock itch or within 4 weeks for athlete's foot and ringworm. Do not use on children under 2 of age except under the advice and supervision of a doctor. If swallowed, get medical help or contact a Poison Control Center right away.

FDA lists 7 drug label records with CLOTRIMAZOLE 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 RoyceDerm Antifungal .spray. used for?
clean the affected area and dry thoroughly. apply 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 ofthis product. for athlete's foot: pay special attention to the spaces between the toes; wear well-fitting,ventilated shoes and change shoes & socks at least once daily. for athlete's foot and ringworm,use …

Who makes RoyceDerm Antifungal .spray.?
RoyceDerm LLC is the labeler of record for RoyceDerm Antifungal .spray.. 7 FDA label records share the active ingredient CLOTRIMAZOLE 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 RoyceDerm Antifungal .spray. 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 RoyceDerm Antifungal .spray. 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 CLOTRIMAZOLE 1%?
Yes. 7 FDA drug label records list CLOTRIMAZOLE 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 RoyceDerm Antifungal .spray. 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.