FDA Label for Optase Allegro
View Indications, Usage & Precautions
Optase Allegro Product Label
The following document was submitted to the FDA by the labeler of this product Scope Health 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.
Otc - Active Ingredient
0.35% Hydroxyethyl Cellulose
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
If swallowed get medical
help or contact a poison
control center right away.
Otc - Purpose
Eye Lubricant
Inactive Ingredient
Inactive ingredients: Citric Acid,
Ectoin, Purified Water, Sodium
Chloride, Trisodium Citrate Dihydrate.
Dosage & Administration
Directions:
Put one or two drops in the
affected eyes as needed.
Warnings
Warning
• For external use only.
• If solution changes color or
becomes cloudy, do not use.
To avoid contamination, do
not touch tip to any surface.
After use, shake the bottle
downwards in order to remove
any residual drop that may be left.
Replace cap after using.
Stop use and ask doctor if:
Stop use and ask doctor if
• You feel eye pain.
• Changes in vision occur.
• Redness or irritation of the eye lasts.
• Condition worsens or lasts
more than 72 hours
Indications & Usage
Uses
• For use as a lubricant to prevent
further irritation.
• May be used as a protectant against
further irritation.
• To relieve dryness of the eye.
* Please review the disclaimer below.