Active Ingredient
Propylene glycol 0.6%
Walgreens Lubricant Eye Drops Restorative Performance Solution/ Drops
FDA Label NDC 0363-1474
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Walgreen Company for the product Walgreens Lubricant Eye Drops Restorative Performance (NDC 0363-1474). 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, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Lubricant
Uses
- For temporary relief of burning and irritation due to dryness of the eye
Warnings
For external use only.
Do not use
- if this product changes color
- if you are sensative to any ingredient in this product
When Using This Product
- do not touch tip of container to any surface to avoid contamination
- replace cap after each use
Stop Use And Ask A Doctor If
- you experience eye pain
- changes in vision occur
- redness or irritation of the eye(s) gets worse, persists or lasts more than 72 hours
Keep Out Of Reach Of Children
- if swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Shake well before using.
- Instill 1 or 2 drops in the affected eye(s) as needed.
Other Information
- Store at room temperature.
Inactive Ingredients
Benzalkonium chloride, boric acid, castor oil, disodium edetate hydrate, polyoxyethylene sorbitan monooleate, potassium chloride, purified water, sodium borate, sodium chloride. May contain hydrochloric acid and/or sodium hydroxide to adjust pH.
Questions Or Comments?
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