Dermact

Dermact is an FDA-registered drug product whose active ingredient is LANOLIN. It is labelled by Marie's Original Formulas LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87541-882, application M016, label effective 20260722. It is one of 8 FDA drug label records sharing the active ingredient LANOLIN. 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 LANOLIN are most often described in connection with: helps protect, temporarily protects, minor cuts, relieve chapped, cracked irritated, drying effects, skin exposed, pressure friction. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses Temporarily protects minor cuts, scrapes, and burns. Helps protect and relieve chapped, cracked, or irritated skin. Helps protect against the drying effects of wind and cold. Helps protect skin exposed to pressure, friction, shear, and prolonged moisture.

Directions Clean the affected area before application. Apply a thin layer to the affected area as needed. May be covered with a sterile bandage.

Warnings For external use only.

FDA lists 8 drug label records with LANOLIN 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 Dermact used for?
Uses Temporarily protects minor cuts, scrapes, and burns. Helps protect and relieve chapped, cracked, or irritated skin. Helps protect against the drying effects of wind and cold. Helps protect skin exposed to pressure, friction, shear, and prolonged moisture.

Who makes Dermact?
Marie's Original Formulas LLC is the labeler of record for Dermact. 8 FDA label records share the active ingredient LANOLIN, 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 Dermact 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 Dermact 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 LANOLIN?
Yes. 8 FDA drug label records list LANOLIN 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 Dermact 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.