Dermasporin

LANOLIN TOPICAL HUMAN OTC DRUG

Dermasporin is an FDA drug label for the active ingredient LANOLIN manufactured by Marie's Original Formulas LLC administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260722.

Generic name
LANOLIN
Manufacturer
Marie's Original Formulas LLC
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
87541-507
Application
M016
Label effective
20260722

About this product

Dermasporin 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 87541-507, 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.

What it is used for

Across FDA labelling, products containing LANOLIN are most often described in connection with: usage helps, temporarily protect, minor cuts. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Indications & Usage

Usage • Helps temporarily protect minor cuts, scrapes, and burns.

Dosage & Administration

Directions • Clean the affected area. • Apply as needed. • May be covered with a sterile bandage.

Warnings

Warnings For external use only. Do not use • On deep or puncture wounds. • On animal bites. • On serious burns. When using this product • Do not get into eyes. 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.

More products with the same ingredient

LANOLIN

ClaraVie

Gentell LLC View label

Claravie

Gentell LLC View label

Dermact

Marie's Original Formulas LLC View label

Dr Sosnowskis Chafing Hero Severe Chafing Balm

Herstat (USA) Inc. View label

Skin Protectant with Lanolin

McKesson View label

Skin Protectant with Lanolin

McKesson Medical-Surgical Inc. View label

Theriac Advanced Healing

Sheffield Pharmaceuticals LLC View label

How products containing LANOLIN compare

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.

Dosage formProductsManufacturerProducts
— — Gentell LLC 2
— — Marie's Original Formulas LLC 2
— — Herstat (USA) Inc. 1
— — McKesson 1
— — McKesson Medical-Surgical Inc. 1

Frequently asked questions

What is Dermasporin used for?
Usage • Helps temporarily protect minor cuts, scrapes, and burns.

Who makes Dermasporin?
Marie's Original Formulas LLC is the labeler of record for Dermasporin. 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 Dermasporin 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 Dermasporin 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 Dermasporin 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.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.