dermveda RINGWORM

dermveda RINGWORM is an FDA-registered drug product whose active ingredient is CARDIOSPERMUM, CURCUMA LONGA. It is labelled by Celcius Corp. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 83819-381, label effective 20260811. It is one of 4 FDA drug label records sharing the active ingredient CARDIOSPERMUM, CURCUMA LONGA. 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 CARDIOSPERMUM, CURCUMA LONGA are most often described in connection with: temporarily relieves, swelling itching, rash skin, irritation inflammation. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses • Temporarily relieves swelling, itching, rash or skin irritation/inflammation.

Directions Do Not use on Children less than 2 Years Please perform a patch test for sensitive skin. Take a small amount with your finger and gently apply it on the affected area. Apply Liberally and use often till symptoms subside.

Warnings For external use only. Do not use • on children under 2 years of age unless directed by a doctor • Avoid contact with eyes. When using this product • Mild increase in irritation or burning may occur. Stop use and ask a doctor if • If symptoms persist or inflammation increases after weeks of use or if the itch increases. • Increase in redness on skin. Pregnant or Breast Feeding • Ask a Health Professional before use. Keep out of reach of children. If swallowed, get medical help or contact a poison Control Center right away.

FDA lists 4 drug label records with CARDIOSPERMUM, CURCUMA LONGA 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 dermveda RINGWORM used for?
Uses • Temporarily relieves swelling, itching, rash or skin irritation/inflammation.

Who makes dermveda RINGWORM?
Celcius Corp. is the labeler of record for dermveda RINGWORM. 4 FDA label records share the active ingredient CARDIOSPERMUM, CURCUMA LONGA, 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 dermveda RINGWORM 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 dermveda RINGWORM 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 CARDIOSPERMUM, CURCUMA LONGA?
Yes. 4 FDA drug label records list CARDIOSPERMUM, CURCUMA LONGA 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 dermveda RINGWORM 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.