Otc - Active Ingredient
Polyethylene Glycol 400, Propylene Glycol
Sysfol Eye Drops
FDA Label NDC 73669-013
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Unimed Pharmaceuticals, Inc. for the product Sysfol Eye Drops (NDC 73669-013). 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, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
boric acid, hypromellose, potassium chloride, purified water, sodium chloride, sodium hyaluronate, sodium, hydroxide
Otc - Purpose
for use as a protectant against further irritation or to relieve dryness of the eye
Otc - Keep Out Of Reach Of Children
keep out of reach of the children
Indications & Usage
Instill 1 or 2 drops in the affectd eye(s) as needed
Warnings
For external use only
When using this product
■ do not touch tip of container to any surface to avoid contamination
■ replace cap after each use
Dosage & Administration
external use only
Package Label.Principal Display Panel
Label (Label)
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