Label: OLOPATADINE HYDROCHLORIDE OPHTHALMIC SOLUTION- olopatadine hydrochloride ophthalmic solution
- NDC Code(s): 83324-120-25
- Packager: Chain Drug Marketing Association INC
- This is a repackaged label.
- Source NDC Code(s): 43598-764
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated September 3, 2024
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- Official Label (Printer Friendly)
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ACTIVE INGREDIENTOlopatadine (0.2%) (equivalent to olopatadine hydrochloride 0.222%)
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PURPOSEAntihistamine
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USEtemporarily relieves itchy eyes due to pollen, ragweed, grass, animal hair and dander
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WARNINGSFor external use only
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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
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WHEN USING THIS PRODUCTdo 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 ...
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STOP USE AND ASK DOCTOR IFyou experience: eye pain - changes in vision - increased redness of the eye - itching worsens or lasts for more than 72 hours
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KEEP OUT OF REACH OF CHILDRENIf swallowed, get medical help or contact a Poison Control Center right away.
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DIRECTIONSadults 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 ...
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OTHER INFORMATION• only for use in the eye • store between 2° to 25°C (36° to 77°F)
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INACTIVE INGREDIENTSBenzalkonium chloride 0.01%, Dibasic sodium phosphate, Edetate disodium, Hydrochloric acid/Sodium hydroxide (adjust pH), Povidone, Sodium chloride, and Water for Injection.
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QUESTIONS?Call 1-888-375-3784
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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
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INGREDIENTS AND APPEARANCEProduct Information