Active Ingredient(S)
Olopatadine 0.2%................ (equivalent to olopatadine hydrochloride 0.222%)
The following Structured Product Label (SPL) was submitted to the FDA by Alembic Pharmaceuticals Limited for the product Olopatadine Hydrochloride (NDC 46708-710). 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(s), purpose, use(s), warnings, do not use, when using this product, stop use and ask doctor if, keep out of 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
you experience:
• eye pain
• changes in vision
• increased redness of the eye
• itching worsens or lasts for more than 72 hours
If swallowed, get medical help or contact a Poison Control Center right away.
•adults and children 2 years of age and older:
•children under 2 years of age: consult a doctor
• only for use in the eye
• store between 2°C to 25°C (36°F to 77°F)
benzalkonium chloride 0.01%, dibasic sodium phosphate, edetate disodium, hydrochloric acid/sodium hydroxide (adjust pH), povidone, sodium chloride, and water for Injection.
Contact Alembic Pharmaceuticals Inc. at 1-866-210-9797
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