FDA Label for Lubricant Eye Drops
View Indications, Usage & Precautions
Lubricant Eye Drops Product Label
The following document was submitted to the FDA by the labeler of this product Oliver Landon Intl Inc.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient
Carboxymethylcellulose sodium 0.5%
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.▪ protects against further irritation.
Warnings
For external use only
Do not use if solution changes color or becomes cloudy
When using this product
▪ do not touch tip of container to any surface to avoid contamination.▪ do not reuse. Once opened, discard.
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.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
• To open, TWIST AND PULL TAB TO REMOVE.• Instill 1 or 2 drops in the affected eye(s) as needed and discard container.
*If used for post-operative dryness and discomfort, follow your eye doctor’s instructions.
Other Information
▪ use before expiration date marked on container.▪ store at 59°-86°F (15°-33°C)
RETAIN THIS CARD FOR FUTURE REFERENCE.
Use only if single-use container is intact.
Inactive Ingredients
Calcium chloride, magnesium chloride, potassium chloride, purified water, sodium chloride and sodium lactate.
May also contain hydrochloric acid and/or sodium hydroxide to adjust pH.
Questions Or Comments?
1 (800) 839-5929
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Lubricant Eye Drops
0.4 ml (0.014 fl oz) per vial
* Please review the disclaimer below.