Active Ingredient
Olopatadine (0.2%)
(equivalent to olopatadine hydrochloride 0.222%)
The following Structured Product Label (SPL) was submitted to the FDA by Bausch & Lomb Incorporated for the product Olopatadine Hydrochloride (NDC 24208-967). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, do not use, when using this product, stop use and ask a doctor if you experience:, keep out reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Olopatadine (0.2%)
(equivalent to olopatadine hydrochloride 0.222%)
Antihistamine
temporarily relieves itchy eyes due to pollen, ragweed, grass, animal hair and dander
For external use only
If swallowed, get medical help or contact a Poison Control Center right away.
benzalkonium chloride 0.01%, dibasic sodium phosphate, edetate disodium, hydrochloric acid/sodium hydroxide (to adjust pH), povidone, sodium chloride and water for injection
Call 1-800-553-5340
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