Otc - Active Ingredient
Lanolin 50%
Skin Protectant With Lanolin Cream
FDA Label NDC 68599-6202
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Mckesson Medical-surgical Inc. for the product Skin Protectant With Lanolin (NDC 68599-6202). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, indications & usage, otc - keep out of reach of children, dosage & administration, inactive ingredient, warnings, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose: Skin protectant
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
Otc - Keep Out Of Reach Of Children
Keep out of the reach of children
If swallowed get medical help or contact a poison control center right away
Dosage & Administration
Gently cleanse and dry area. Apply as needed to affected area.
Inactive Ingredient
Inactive Ingredient:
Aloe Barbadensis Leaf Juice
Beeswax (Yellow Wax)
Disodium EDTA
Lanolin Alcohol
Mineral Oil
Petrolatum
Phenoxyethanol
Caprylyl Glycol
Sodium Borate
Sorbitan Sesquioleate
Water
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
* Please review the disclaimer below.
