Warnings
- For use in the eyes only.
- Save box for complete information.
Vedlube Ointment
FDA Label NDC 50989-476
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Vedco Inc for the product Vedlube (NDC 50989-476). 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 warnings, active ingredients, inactive ingredients, purpose, uses, when using this product, stop use and ask a doctor if, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Mineral Oil 15%
White Petrolatum 85%
Inactive Ingredients
Lanolin Alcohols
Purpose
Eye Lubricant
Uses
- as a lubricant to prevent further irritation
- to relieve dryness of the eye(s)
When Using This Product
- avoid contamination, do not touch tip of container to any surface.
- replace cap after each use.
Stop Use And Ask A Doctor If
- you experience eye pain, changes in vision, continued redness or irritation of the eye.
- condition worsens or persists for more than 72 hours.
Directions
- pull down lower lid of the affected eye and apply a small amount (one-fourth inch) of ointment to the inside of the eyeid every 3-4 hours or as directed by a doctor.
Other Information
- store at room temperature 15° - 30°C (59° - 86°F).
- protect from freezing.
- see crimp of tube or box for lot number and expiration date.
- keep tightly closed.
- does not contain preservatives.
Questions Or Comments?
- 888-708-3326
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