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.
Optase Solution/ Drops
FDA Label NDC 72972-008
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 72972-008). 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 - keep out of reach of children, otc - active ingredient, otc - purpose, inactive ingredient, dosage & administration, warnings, indications & usage, immediate label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
0.3 % glycerin
Otc - Purpose
Eye Lubricant
Inactive Ingredient
Inactive Ingredients
Borax, Boric Acid, Citric Acid anhydrous,
Sodium Chloride, Sodium Citrate Dihydrate, Sodium Hyaluronate, water.
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 of container to any surface. Replace cap after using.
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.
