Active Ingredient
Lanolin 22%
Lincofix
FDA Label NDC 69636-8050
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Lincoln Pharmaceuticals Ltd. for the product Lincofix (NDC 69636-8050). 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 active ingredient, purpose, uses, warnings, when using this product, stop use and ask a doctor if, do not use on, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Skin Protectant
Uses
- Helps prevent and temporarily protects chafed, chapped or cracked skin
- Temporarily protects minor cuts, scrapes, burns
Warnings
FOR EXTERNAL USE ONLY
When Using This Product
- Avoid contact with eyes
- If contact occurs, flush with water
Stop Use And Ask A Doctor If
- condition worsens
- symptoms last more than seven days or clear up and occur again within seven days
Do Not Use On
- deep or puncture wounds
- lacerations
- animal bites
- serious burns
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away
Directions
Apply as needed to clean skin twice daily or more often if necessary
- For Children under 6 months ask a doctor
Inactive Ingredients
Aluminium Hydroxide, Alpha Tocopherol Acetate(Vitamin E), Calcium carbonate, Cholecalciferol (Vitamin D3), Citric Acid,Corn Oil, Ethylparaben, Lanolin, Magnesium Hydroxide, Methylparaben, Sodium Chloride, Sodium laureth Sulfate, Petrolatum, Vitamin A Palmitate, Water, Zinc Chloride
Package Label.Principal Display Panel
Product Label (11 80502ln 01)
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