Olopatadine Hydrochloride Solution/ Drops
Product Images NDC 60505-6222

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Olopatadine Hydrochloride (NDC 60505-6222). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Apotex Corp., 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

Bottle Label (Bottle Label)

Label for Olopatadine HCl Ophthalmic Solution USP 0.2%, an eye drop solution containing 2 mg/mL olopatadine hydrochloride. The label indicates a 2.5 mL bottle size and highlights once daily use for eye allergy itch relief. It is sterile and classified as an antihistamine. The product is labeled by Apotex Corp., with storage instructions and tamper-evident warnings included.*

FDA Label Image

Carton Label (Carton Label)

Packaging label for Olopatadine hydrochloride 0.2% ophthalmic solution drops by Apotex Corp. The carton indicates it is an antihistamine for eye allergy itch relief, available without prescription in a 2.5 mL (0.085 FL OZ) sterile solution. It includes drug facts, usage directions, inactive ingredients, warnings, and tamper-evident information. The label also shows the NDC 60505-6222-2 and manufacturer details for Apotex Inc., Toronto.*

* 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.