Skin Protectant with Lanolin

LANOLIN TOPICAL HUMAN OTC DRUG

Skin Protectant with Lanolin is an FDA drug label for the active ingredient LANOLIN manufactured by McKesson Medical-Surgical Inc. 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 20260708.

Generic name
LANOLIN
Manufacturer
McKesson Medical-Surgical Inc.
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
68599-6202
Application
M016
Label effective
20260708

About this product

Skin Protectant with Lanolin is an FDA-registered drug product whose active ingredient is LANOLIN. It is labelled by McKesson Medical-Surgical Inc. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 68599-6202, application M016, label effective 20260708. 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: temporarily protects, minor cuts, helps relieve, chafed chapped, cracked skin, prevent incontinence, associated dermatitis. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Lanolin 50%

Indications & Usage

Temporarily protects minor cuts, scrapes and burns Temporarily protects and helps relieve chafed, chapped or cracked skin and lips Helps prevent incontinence -associated dermatitis

Dosage & Administration

Gently cleanse and dry area. Apply as needed to affected area.

Warnings

For external use only When using this product, do not get into eyes Stop use and ask doctor if condition lasts more than 7 days Do not use on deep or punture wounds, animal bites, serious burns

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

Dermasporin

Marie's Original Formulas LLC View label

Dr Sosnowskis Chafing Hero Severe Chafing Balm

Herstat (USA) 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

Recall and safety notices

5 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.

RecallProductFirmClassStatusReported
D-0538-2025 PROLIA (denosumab), injection, 60mg/mL, For Subcutaneous Use Only, Rx Only, Manufactured by: Amgen Inc., Thousand Oaks, CA 91320, NDC 55513-710-21 Mckesson Medical-Surgical Inc. Corporate Office Class II Ongoing 20250730
D-0540-2025 BENLYSTA (belimumab) for injection, 400 mg/20 mL vial, Rx only, NDC 49401-102-01, GSK. Mckesson Medical-Surgical Inc. Corporate Office Class II Ongoing 20250730
D-0539-2025 EVENITY, (romosozumab -aqqg) injection, 105mg/1.17 mL, For Subcutaneous Use Only, Rx Only, Manufactured by: Amgen Inc., Thousand Oaks, CA 91320, NDC 55513-880-02. Mckesson Medical-Surgical Inc. Corporate Office Class II Ongoing 20250730
D-0401-2025 Infuvite Adult, multiple vitamins injection, Baxter, Five of Vial 1 (5 mL) and Five of Vial 2 (5mL), Rx Only, Sterile, Manufactured for: Sandoz Inc., Princeton, NJ 08540, Distributed by Baxter Healthcare Corporation, Deerfield, IL 60015 USA, Product of Canada, NDC 54643-5649-1 Mckesson Medical-Surgical Inc. Corporate Office Class II Ongoing 20250507
D-0400-2025 Medroxyprogesterone Acetate Injectable Suspension, USP, 150 mg / mL, 1 mL Single-Dose Vial, Rx only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ 08520, NDC 55150-0330-01 Mckesson Medical-Surgical Inc. Corporate Office Class II Ongoing 20250507

Frequently asked questions

What is Skin Protectant with Lanolin used for?
Temporarily protects minor cuts, scrapes and burns Temporarily protects and helps relieve chafed, chapped or cracked skin and lips Helps prevent incontinence -associated dermatitis

Who makes Skin Protectant with Lanolin?
McKesson Medical-Surgical Inc. is the labeler of record for Skin Protectant with Lanolin. 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 Skin Protectant with Lanolin 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 Skin Protectant with Lanolin 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 Skin Protectant with Lanolin been recalled?
5 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.

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.