Olopatadine Solution/ Drops
Product Images NDC 70069-017

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Olopatadine (NDC 70069-017). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Somerset Therapeutics, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

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Label for Olopatadine Hydrochloride Ophthalmic Solution USP 0.1%, an antihistamine and redness reliever eye drop solution. The label indicates a 5 mL (0.17 FL OZ) bottle, sterile, for ophthalmic use only, intended for twice daily relief of eye allergy itch and redness. Manufactured by Somerset Therapeutics, LLC, Somerset, NJ, and made in India. Storage conditions and tamper-evident instructions are included. The NDC is 70069-017-01.*

FDA Label Image

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The packaging label for Olopatadine Hydrochloride Ophthalmic Solution USP, 0.1%, by Somerset Therapeutics, LLC. It is an antihistamine and redness reliever eye drop solution for ophthalmic use, indicated for eye allergy itch and redness relief. The label highlights twice daily relief, a 5 mL bottle size (0.17 FL OZ), and states it is sterile. Additional details include usage instructions, warnings, and inactive ingredients.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.