Active Ingredient
Olopatadine (0.1%)
(equivalent to olopatadine hydrochloride, USP 0.111%)
The following Structured Product Label (SPL) was submitted to the FDA by Sola Pharmaceuticals for the product Olopatadine Hcl (NDC 70512-520). 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 our of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Olopatadine (0.1%)
(equivalent to olopatadine hydrochloride, USP 0.111%)
Antihistamine and redness reliever
Temporarily relieves itchy and red 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.
consult a doctor
benzalkonium chloride 0.01%, dibasic sodium phosphate, hydrochloric acid/sodium hydroxide (to adjust pH), sodium chloride and water for injection
Call 1-866-747-7365
Manufactured for:
SOLA Pharmaceuticals LLC,
Baton Rouge, LA 70810
Made in India
Code No: DD/DRUGS/DD/292
Olopatadine Hcl Opthalmic Solution 0.1% Bottle Label:
Olopatadine Hcl Opthalmic Solution 0.1% Carton Label:
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