FDA Label for Equaline Lubricant Eye Drops
View Indications, Usage & Precautions
Equaline Lubricant Eye Drops Product Label
The following document was submitted to the FDA by the labeler of this product United Natural Foods, 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 Ingredients
Polyethylene glycol 0.4%
Propylene glycol 0.3%
Purposes
Lubricant
Lubricant
Use
- for use as a protectant against further irritation or to relieve dryness of the eye
Warnings
For external use only
Do Not Use
- if this product changes color or becomes cloudy
- if you are sensitive 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 Any Of The Following:
- eye pain
- changes in vision occur
- 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 (1-800-222-1222) right away.
Directions
put 1 or 2 drops in the affected eye(s) as needed
Other Information
Store at 15°-25°C (59°-77°F)
Inactive Ingredients
boric acid, hypromellose, potassium chloride, purified water, sodium chloride, sodium hyaluronate, sodium hydroxide
Questions Or Comments?
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