Label: OLOPATADINE HYDROCHLORIDE OPHTHALMIC SOLUTION- olopatadine hydrochloride ophthalmic solution

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated September 3, 2024

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  • 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 ...
  • 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 ...
  • 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 1-888-375-3784
  • PRINCIPAL DISPLAY PANEL(What is this?)
    NDC 83324-120-25 - Olopatadine Hydrochloride - Ophthalmic Solution, USP - 0.2% Bottle Label: Olopatadine Hydrochloride - Ophthalmic Solution, USP - 0.2% Carton Label
  • INGREDIENTS AND APPEARANCE
    Product Information