FDA Label for Well Lubricant Eye Drops
View Indications, Usage & Precautions
Well Lubricant Eye Drops Product Label
The following document was submitted to the FDA by the labeler of this product True Marker Pharmaceuticals, 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 (S) Purpose
Propylene Glycol 0.7% Lubricant
Uses
- for the temporary relief of burning and irritation due to dryness of the eye
- for the temporary relief of discomfort due to minor irritations of the eye or to exposureto wind or sun
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
- to avoid contamination do no touch tip of container to any surface
- replace cap after each use
- remove contact lenses before use
- eye pain
- change in vision
- continued redness or irritation of the eye
- condition worsens or persisters for more than 72 hours
When using this product
Stop use and ask a doctor if you experience any of the
following:
Keep out of reach of children. If swallowed, get medica-l help or contact a Poison Control Center right (1-800-222-1222) away.
Directions
- Shake well before using.
- Put 1 or 2 drops in the affected eye (s) as needed.
Other Information
store at 15°-30°C (59°-86°F)
Inactive Ingredients
Water, Boric Acid, Potassium Chloride, Sorbitol, Glycerin, Hyluronic Acid, Amynomethylpropanol, Benzalhonium Chloride, Sodium Chorlide, Hydrochloric Acid, Sodium Hydroxide
Questions?
1-888-811-2634.
Product Label
* Please review the disclaimer below.
