DeFlame

DeFlame is an FDA-registered drug product whose active ingredient is ALLANTOIN. It is labelled by Noon Aesthetics M.R. Ltd taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 78863-1270, application M020, label effective 20260728. It is one of 9 FDA drug label records sharing the active ingredient ALLANTOIN. 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 ALLANTOIN are most often described in connection with: temporarily protects, minor skin, irritation cuts, scrapes burns, helps protect, relieve chafed, chapped cracked. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses Temporarily protects minor: skin irritation, cuts, scrapes, burns and helps protect and relieve chafed, chapped or cracked skin.

Directions Apply as needed.

Warnings For external use only. Do not use on deep or puncture wounds, animal bites, serious burns. When using this product avoid contact with eyes. In case of eye contact, flush with water. Stop use and ask a doctor if condition worsens symptoms last more than 7 days or clear up and occur again within a few days. Keep out of reach of children.

FDA lists 9 drug label records with ALLANTOIN 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 DeFlame used for?
Uses Temporarily protects minor: skin irritation, cuts, scrapes, burns and helps protect and relieve chafed, chapped or cracked skin.

Who makes DeFlame?
Noon Aesthetics M.R. Ltd is the labeler of record for DeFlame. 9 FDA label records share the active ingredient ALLANTOIN, 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 DeFlame 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 DeFlame 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 ALLANTOIN?
Yes. 9 FDA drug label records list ALLANTOIN 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 DeFlame 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.