Active Ingredient
Carboxymethylcellulose sodium 1%
Lubricant Eye
FDA Label NDC 76168-351
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Velocity Pharma Llc for the product Lubricant Eye (NDC 76168-351). 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, directions, other information, inactive ingredients, 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
Purpose
Eye lubricant
Uses
- For the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun.
- May be used as a protectant against further irritation.
Warnings
- For external use only.
- To avoid contamination, do not touch tip of container to any surface. Replace cap after using.
- If solution changes color or becomes cloudy, do not use.
Directions
Instill 1 or 2 drops in the affected eye(s) as needed.
Other Information
- Use before expiration date marked on container.
- Discard 30 days after opening.
- Store at 59°-86°F (15°-30°C).
- RETAIN THIS CARTON FOR FUTURE REFERENCE.
Inactive Ingredients
Boric acid; calcium chloride; magnesium chloride; potassium chloride; purified water; stabilized oxychloro complex; and sodium chloride.
May contain hydrochloric acid and/or sodium hydroxide to adjust pH
Package Label.Principal Display Panel
2 (2)
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