Olopatadine Hydrochloride Solution
Product Images NDC 46122-672

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Olopatadine Hydrochloride (NDC 46122-672). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amerisource Bergen, 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

Package Label-principal Display Panel-0.1% (5 mL Container) (Olopatadine Fig1)

Package Label-principal Display Panel-0.1% (5 mL Container) (Olopatadine Fig1)
Label for Olopatadine Hydrochloride Ophthalmic Solution USP 0.1%, an eye drop solution for allergy itch and redness relief. The 5 mL (0.17 FL OZ) sterile solution is labeled with storage instructions and tamper-evident warnings. Distributed by AmerisourceBergen.*
FDA Label Image

Package Label-principal Display Panel-0.1% (5 mL Container Carton) (Olopatadine Fig2)

Package Label-principal Display Panel-0.1% (5 mL Container Carton) (Olopatadine Fig2)
The packaging label for Olopatadine Hydrochloride Ophthalmic Solution, USP 0.1%, an eye drop solution by Amerisource Bergen under Good Neighbor Pharmacy branding. The sterile 5 mL (0.17 fl oz) bottle provides twice daily relief from eye allergy itch and redness caused by allergens such as pet dander, pollen, grass, and ragweed. The label includes Drug Facts with active ingredient details, usage instructions, warnings, inactive ingredients, and distributor information. It also notes this product is not manufactured or distributed by the Pataday® trademark holder and is a 30-day supply for ages 2 and older.*

* 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.