Label: OLOPATADINE HYDROCHLORIDE solution
- NDC Code(s): 82442-966-01
- Packager: TARGET CORPORATION
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated January 28, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
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 useif 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 ...
-
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 ...
-
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, hydrochloric acid/sodium hydroxide (to adjust pH), sodium chloride and water for injection
-
Questions?
Call1-800-910-6874
-
Package/Label Principal Display Panel
-
INGREDIENTS AND APPEARANCEProduct Information