FDA Label for Olopatadine Hydrochloride Ophthalmic Solution

View Indications, Usage & Precautions

Olopatadine Hydrochloride Ophthalmic Solution Product Label

The following document was submitted to the FDA by the labeler of this product Target Corporation. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.

Active Ingredient



Olopatadine (0.1%) (equivalent to olopatadine hydrochloride 0.111%)


Purpose



Antihistamine and redness reliever



Uses



temporarily relieves itchy and red 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) twice daily, every 6 to 8 hours, no more than twice 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° to 25°C (39° to 77°F)


Inactive Ingredients



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


Questions?



Call 1-888-375-3784


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