Olopatadine Hydrochloride Solution
Product Images NDC 16571-882

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Olopatadine Hydrochloride (NDC 16571-882). 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

Carton-label.jpg (Carton Label)

Packaging label for Olopatadine Hydrochloride Ophthalmic Solution, USP 0.1%, a sterile 5 mL (0.17 FL OZ) solution by Rising Pharma Holdings, Inc. This OTC eye drop provides relief for eye allergy itch and redness, intended for ages 2 and older with a 30 day supply. The label includes tamper-evident instructions and detailed drug facts covering active ingredients, uses, warnings, directions, and inactive ingredients.*

FDA Label Image

Container-label.jpg (Container Label)

Label for Olopatadine Hydrochloride Ophthalmic Solution, USP 0.1%, 5 mL (0.17 FL OZ) sterile eye drops. The label shows dosing as twice daily, indicates it relieves eye allergy itch and redness, and includes tamper-evident instructions. Manufactured for Rising Pharma Holdings, Inc., East Brunswick, NJ, made in India, with NDC 16571-882-05.*

* 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.