Otc - Active Ingredient
Glycerin 0.9%
Optase Solution/ Drops
FDA Label NDC 72972-004
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 (NDC 72972-004). 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, warnings, indications & usage, dosage & administration, inactive ingredient, other safety information, 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
Warnings
Warning
• For external use only.
• To avoid contamination, do not touch tip
of container to any surface. After use, shake the bottle
downwards in order to remove any residual drop that
may be left. Replace cap after using.
• Do not use the solution if it changes color or becomes
cloudy
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.
Dosage & Administration
Directions
Put one or two drops in the affected eyes as needed.
Inactive Ingredient
Citric Acid Monohydrate, Polyoxyethylenesorbitan Monooleate, Potassium Chloride, Purified Water, Saccha Inchi Seed Oil, Sodium Hyaluronate , Sorbitan Monooleate, Trehalose, Tromethamine
* Please review the disclaimer below.
