SUPRADERM
SUPRADERM is an FDA drug label for the active ingredient WHITE PETROLATUM, LANOLIN manufactured by Olen Skin Care Corporation 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 20260610.
- Generic name
- WHITE PETROLATUM, LANOLIN
- Manufacturer
- Olen Skin Care Corporation
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 52358-0002
- Application
- M016
- Label effective
- 20260610
About this product
SUPRADERM is an FDA-registered drug product whose active ingredient is WHITE PETROLATUM, LANOLIN. It is labelled by Olen Skin Care Corporation taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 52358-0002, application M016, label effective 20260610. 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 WHITE PETROLATUM, LANOLIN are most often described in connection with: temporarily protects, minor cuts, scrapes burns, helps relieve, chapped cracked, drying effects, cold weather. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses Temporarily Protects Minor: Cuts Scrapes Burns Temporarily protects and helps relieve chapped or cracked skin Helps protect from the drying effects of wind and cold weather
Dosage & Administration
Directions Apply as needed.
Warnings
Warnings For External Use Only Do not use on deep or puncture wounds animal bites 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 Keep out of the reach of chilren . If swallowed, get mdical help or contact a poison control center right away.
Frequently asked questions
What is SUPRADERM used for?
Uses Temporarily Protects Minor: Cuts Scrapes Burns Temporarily protects and helps relieve chapped or cracked skin Helps protect from the drying effects of wind and cold weather
Who makes SUPRADERM?
Olen Skin Care Corporation is the labeler of record for SUPRADERM.
What form does SUPRADERM 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 SUPRADERM 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.
Has SUPRADERM 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.