FDA Label for Lubricant Drops
View Indications, Usage & Precautions
Lubricant Drops Product Label
The following document was submitted to the FDA by the labeler of this product Cardinal Health, 110 Dba Leader. 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.
- For use as a protectant against further irritation or to relieve dryness of the eye.
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.
Stop Use And Ask A Doctor If
you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the 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
Instill 1 or 2 drops in the affected eye(s) as needed.
Other Information
- Use only if imprinted tape seals on top and bottom flaps are intact and clearly legible.
- Use before expiration date marked on container.
- Discard 90 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 also contain hydrochloric acid and/or sodium hydroxide to adjust pH.
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