Olopatadine Hydrochloride Ophthalmic Solution
Product Images NDC 63868-821

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Olopatadine Hydrochloride Ophthalmic Solution (NDC 63868-821). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chain Drug Marketing Association Inc, 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

Carton (Carton)

Packaging label for Olopatadine Hydrochloride Ophthalmic Solution USP 0.2%, an antihistamine eye drop for allergy relief. The 2.5 mL sterile solution is labeled for once daily use to relieve eye allergy symptoms caused by pet dander, pollen, grass, and ragweed. Distributed by Chain Drug Marketing Association Inc, the label features drug facts with usage directions, warnings, and inactive ingredients, including benzalkonium chloride and dibasic sodium phosphate. The label also includes barcodes and storage instructions (store between 2°-25°C).*

FDA Label Image

Container (Container)

Label for Olopatadine Hydrochloride Ophthalmic Solution USP 0.2% (2 mg/mL) in a 2.5 mL sterile solution. It is described as an antihistamine providing once daily relief for eye allergy itch. The label indicates storage conditions, tamper-evident packaging, and distribution by Dr. Reddy's Laboratories, Inc., made in India.*

* 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.