Active Ingredient
Ketotifen 0.025%
(equivalent to ketotifen fumarate 0.035%)
The following Structured Product Label (SPL) was submitted to the FDA by Walgreen Company for the product Eye Itch Relief (NDC 0363-0038). 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 active ingredient, purpose, uses, warnings, keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Ketotifen 0.025%
(equivalent to ketotifen fumarate 0.035%)
Antihistamine
For the temporary relief of itchy eyes due to ragweed, pollen, grass, animal hair and dander.
For external use only
Do not use
■ if you are sensitive to any ingredient in this product
■ if solution changes color or becomes cloudy
■ to treat contact lens related irritation
When using this product
■ remove contact lenses before use
■ wait at least 10 minutes before re-inserting content lenses after use
■ do not touch tip of container to any surface to avoid contamination
■ replace cap after each use
Stop use and ask a doctor if you experience any of the following: ■ eye pain ■ changes in vision ■ redness of the eyes ■ itching that worsens or lasts for more than 72 hours
If swallowed, get medical help or contact a Poison Control Center right away.
Adults and children 3 years and older: put 1 drop in the affected eye(s) twice daily, every 8-12 hours, no more than twice per day.
Children under 3 years of age: consult a doctor
Store at 4-25°C (39-77°F)
benzalkonium chloride 0.01%, glycerin, hydrochloric acid and/or sodium hydroxide, water for injection
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