Olopatadine Hydrochloride Solution
Product Images NDC 58602-012

2 FDA label images from Aurohealth Llc · 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 58602-012). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurohealth Llc, 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

Package Label-principal Display Panel-0.1% (5 mL Container) (Olopatadine Fig1)

Package Label-principal Display Panel-0.1% (5 mL Container) (Olopatadine Fig1)
Label for Olopatadine Hydrochloride Ophthalmic Solution USP 0.1%, an antihistamine and redness reliever eye drop solution. The sterile product is in a 5 mL (0.17 FL OZ) bottle, intended for ophthalmic use, providing eye allergy itch and redness relief. Distributed by Aurohealth LLC, made in India, with storage instructions and tamper-evident warning included.*
FDA Label Image

Package Label-principal Display Panel-0.1% (5 mL Container Carton) (Olopatadine Fig2)

Package Label-principal Display Panel-0.1% (5 mL Container Carton) (Olopatadine Fig2)
Packaging label for Olopatadine Hydrochloride Ophthalmic Solution USP 0.1% by Aurohealth LLC. This OTC eye drop solution is presented in a 5 mL (0.17 FL OZ) bottle, designed for twice-daily use to relieve eye allergy itch and redness caused by allergens like pet dander, pollen, grass, and ragweed. The label includes directions, warnings, inactive ingredients, storage instructions, and a barcode.*

* 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.