Olopatadine Hydrochloride Solution
Product Images NDC 16571-861

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Olopatadine Hydrochloride (NDC 16571-861). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rising Pharma Holdings, 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

Olapatadine-0.2-carton.jpg (Olapatadine 0.2 Carton)

Packaging label for Olopatadine Hydrochloride Ophthalmic Solution, USP 0.2%, 2.5 mL sterile solution, by Rising Pharma Holdings, Inc. The label shows product information including active ingredient olopatadine hydrochloride 0.2%, purpose as antihistamine, usage instructions, and warnings. It specifies a 30-day supply and includes barcodes and lot/expiration placeholders. The design features the Rising Pharma logo and highlights once daily relief from allergies.*

FDA Label Image

Olapatadine-0.2-container.jpg (Olapatadine 0.2 Container)

Label for Olopatadine Hydrochloride Ophthalmic Solution USP 0.2%, 2.5 mL sterile eye drop solution by Rising Pharma Holdings, Inc. The label includes storage instructions, tamper-evident warning, barcodes, and indicates the product is for eye allergy itch relief and antihistamine use. Manufactured in India, issued November 2024.*

* 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.