Olopatadine Hydrochloride Solution/ Drops
Product Images NDC 51407-663

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 51407-663). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Golden State Medical Supply, 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

51407-663-05 Container.jpg (51407 663 05 Container)

51407-663-05 Container.jpg (51407 663 05 Container)
Label for Olopatadine hydrochloride ophthalmic solution USP 0.1% sterile eye drops, 5 mL (0.17 FL OZ). The label includes dosing instructions indicating use twice daily, and describes the product as an antihistamine and redness reliever for eye allergy itch and redness relief. Manufactured by Apotex Inc. Toronto and marketed by GSMS Incorporated, Camarillo, CA. Storage instructions are 4°C to 25°C (39°F to 77°F). The label also notes tamper-evident packaging.*
FDA Label Image

51407-663-05.jpg (51407 663 05)

51407-663-05.jpg (51407 663 05)
Carton label for Olopatadine hydrochloride Ophthalmic Solution USP 0.1%, a sterile eye drop solution marketed by Golden State Medical Supply, Inc. The 5 mL (0.17 FL OZ) package is labeled as an antihistamine and redness reliever for eye allergy itch and redness relief. The label includes drug facts, active and inactive ingredients, storage instructions, and usage directions, with emphasis on use twice daily for adults and children aged 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.