Olopatadine Hydrochloride Solution
Product Images NDC 58602-007

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Olopatadine Hydrochloride (NDC 58602-007). 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-0.2% (2.5 mL Container) (Olopatadine Fig1)

The label for Olopatadine Hydrochloride Ophthalmic Solution USP 0.2% by Aurohealth LLC. It is an antihistamine sterile eye solution for allergy itch relief, packaged in a 2.5 mL (0.085 FL OZ) container. Instructions designate use only in the eye with storage between 2° to 25°C and tamper-evident warnings. The label includes the NDC 58602-007-39, distributor information, and indicates it is made in India.*

FDA Label Image

Package Label-principal Display Panel-0.2% (2.5 mL Container Carton) (Olopatadine Fig2)

The packaging label for Olopatadine Hydrochloride Ophthalmic Solution, USP 0.2% by Aurohealth LLC. The carton highlights the product as an eye allergy itch relief solution with a 2.5 mL (0.085 FL OZ) sterile solution. The label includes dosing directions, warnings, inactive ingredients, and a tamper-evident feature on the bottle cap image. The product is indicated for relief from pet dander, pollen, grass, and ragweed allergies, with use recommended once daily for ages 2 and older.*

FDA Label Image

Package Label-principal Display Panel-0.2% (2.5 mL Container Carton) Twin Pack (Olopatadine Fig3)

Packaging label for Olopatadine Hydrochloride Ophthalmic Solution, USP 0.2% by Aurohealth LLC. The label shows a twin pack containing two 2.5 mL bottles (each 0.085 FL OZ) of an eye allergy itch relief antihistamine solution. The label mentions the product is sterile, for external use, and provides relief from pet dander, pollen, grass, and ragweed allergies. Additional details include storage instructions, inactive ingredients, and warnings.*

* 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.