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Olopatadine Hydrochloride Ophthalmic Solution

Dosage form
SOLUTION
Labeler
TARGET CORPORATION
Label updated
2025-04-14
Retrieved
2026-09-07
Active ingredients
OLOPATADINE HYDROCHLORIDE
View original label and images on DailyMed ↗
Active ingredient

Olopatadine (0.2%)

(equivalent to olopatadine hydrochloride 0.222%)

Purpose

Antihistamine

Uses

temporarily relieves itchy eyes due to pollen, ragweed, grass, animal hair and dander

Warnings

For external use only

Do not use
  • if solution changes color or becomes cloudy
  • if you are sensitive to any ingredient in this product
  • to treat contact lens related irritation
When using this product
  • do not touch tip of container to any surface to avoid contamination
  • remove contact lenses before use
  • wait at least 10 minutes before reinserting contact lenses after use
  • do not wear a contact lens if your eye is red
Stop use and ask a doctor if you experience:
  • eye pain
  • changes in vision
  • increased redness of the eye
  • itching worsens or lasts for more than 72 hours
Keep out reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions
  • adults and children 2 years of age and older:
  • put 1 drop in the affected eye(s) once daily, no more than once per day
  • if using other ophthalmic products while using this product, wait at least 5 minutes between each product
  • replace cap after each use
  • children under 2 years of age:consult a doctor
Other information
  • only for use in the eye
  • store between 4 25 °C (39 77 °F)
  • protect from light
Inactive ingredients

benzalkonium chloride 0.01%, dibasic sodium phosphate, edetate disodium, hydrochloric acid/sodium hydroxide (to adjust pH), povidone, sodium chloride and water for injection

Questions?

Call 1-800-910-6874

Principle Display Panel

[Image in the official label — see DailyMed source]

NDC: 82442-967-02

20077500
JE61705

DailyMed Set ID: 355df5ce-95e2-4d05-9114-a3190d934d3a · Version 3
NDC: 82442-967