Olopatadine Hydrochloride Solution
Product Images NDC 51407-938

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 51407-938). 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

Carton-olopatadine Hci Opht Soln-5ml_51407-938-05.jpg (Carton Olopatadine Hci Opht Soln 5ml 51407 938 05)

Carton-olopatadine Hci Opht Soln-5ml_51407-938-05.jpg (Carton Olopatadine Hci Opht Soln 5ml 51407 938 05)
Packaging label for OLOPATADINE HCl Ophthalmic Solution USP 0.1%, 5 mL (0.17 FL OZ) by Golden State Medical Supply, Inc. This OTC antihistamine and redness reliever eyedrop provides relief for eye allergy itch and redness caused by allergens such as pet dander, pollen, grass, and ragweed. The label includes usage directions, warnings, inactive ingredients, tamper-evident details, and a barcode with NDC 51407-93805.*
FDA Label Image

Label-olopatadine Hci Opht Soln-5ml_51407-938-05.jpg (Label Olopatadine Hci Opht Soln 5ml 51407 938 05)

Label-olopatadine Hci Opht Soln-5ml_51407-938-05.jpg (Label Olopatadine Hci Opht Soln 5ml 51407 938 05)
Label for Olopatadine Hydrochloride ophthalmic solution 0.1% (1 mg/mL), an antihistamine and redness reliever for eye allergy itch and redness relief. The sterile solution is in a 5 mL (0.17 FL OZ) bottle with tamper-evident packaging. Marketed by GSMS, Incorporated, Camarillo, California, USA, with storage instructions between 4°C and 25°C (39°F to 77°F).*

* 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.