Olopatadine Hydrochloride Solution/ Drops
Product Images NDC 70069-491

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Olopatadine Hydrochloride (NDC 70069-491). 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

Image (F19c5298 B566 4416 A345 C5334c6a7ad7 17)

Label for Olopatadine Hydrochloride Ophthalmic Solution containing 0.2% concentration. It is an antihistamine solution for ophthalmic use, provided in a 2.5 mL (0.085 FL OZ) bottle. The label states 'Once Daily Relief' for eye allergy itch and includes storage instructions, tamper-evident seal notice, and manufacturer information for Somerset Therapeutics, LLC.*

FDA Label Image

Image (F19c5298 B566 4416 A345 C5334c6a7ad7 18)

Packaging label for Olopatadine Hydrochloride Ophthalmic Solution USP 0.2%, a 2 mg/mL antihistamine eye drop solution for once daily relief of eye allergy symptoms. The label indicates it is sterile and for ages 2 and older, with a 2.5 mL (0.085 fl oz) container supplied by Somerset Therapeutics, LLC. The label highlights fast relief from pet dander, pollen, grass, and ragweed allergies.*

* 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.