Otc - Active Ingredient
0.35% Hydroxyethyl Cellulose
Optase Allegro Solution/ Drops
FDA Label NDC 72972-006
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Scope Health Inc for the product Optase Allegro (NDC 72972-006). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - keep out of reach of children, otc - purpose, inactive ingredient, dosage & administration, warnings, indications & usage, patient information leaflet, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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.
