Sunmark Dry Eye Relief
Sunmark Dry Eye Relief is an FDA drug label for the active ingredient GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400 manufactured by Strategic Sourcing Services LLC administered by OPHTHALMIC. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231223.
Generic: GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400
Manufacturer: Strategic Sourcing Services LLC
Product Type: HUMAN OTC DRUG
Route: OPHTHALMIC
Dosage Form:
NDC: 49348-095
Application: M018
Effective: 20231223
Active Ingredients: Active ingredients Glycerin 0.2% Hypromellose 0.2% Polyethylene glycol 1%
Indications & Usage
Uses for the temporary relief of burning and irritation due to dryness of the eye for protection against further irritation
Dosage & Administration
Directions Instill 1 or 2 drops in the affected eye(s) as needed Children under 6 years of age: ask doctor
Contraindications
Not available.
Warnings
Warnings For external use only Do not use this product if solution changes color or becomes cloudy Stop use and ask a doctor if you experience eye pain changes in vision continued redness or irritation of the eye or if the condition worsens or persists for more than 72 hours When using this product to avoid contamination, do not touch tip of container to any surface replace cap after using. Keep container tightly closed remove contact lens before using Keep out of reach of children If accidentally swallowed get medical help or contact a Poison Control Center immediately If pregnant and breast-feeding , ask a health professional before use
Adverse Reactions
Not available.
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