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Eye Allergy Itch Relief Once Daily Relief

Dosage form
SOLUTION
Labeler
Strategic Sourcing Services LLC
Label updated
2025-12-12
Retrieved
2026-09-07
Active ingredients
See original label
View original label and images on DailyMed ↗
Label information

Label information

ACTIVE INGREDIENT

Olopatadine (0.2%)  (equivalent to olopatadine hydrochloride 0.222%)

PURPOSE

Antihistamine

USE

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 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 OF 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 2° to 25°C (36° to 77°F)

INACTIVE INGREDIENTS

Benzalkonium chloride 0.01%, Dibasic sodium phosphate, Edetate disodium, Hydrochloric acid/Sodium hydroxide (adjust pH), Povidone, Sodium chloride, and Water for Injection.

QUESTIONS?

Call 833-358-6431 Monday to Friday 9:00am to 7:00pm EST

PRINCIPAL DISPLAY PANEL


Olopatadine Hydrochloride
Ophthalmic Solution, USP
0.2%

[Image in the official label — see DailyMed source]


DailyMed Set ID: ad35e069-72ba-b8df-d6bd-18c0345c80ac · Version 2
NDC: 70677-1155