Olopatadine Hydrochloride Solution
Product Images NDC 80539-001

2 FDA label images from Allwell Health Inc · 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 80539-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Allwell Health 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

Package Label-principal Display Panel-0.2% (2.5 mL Container) (Olopatadine Fig1)

Package Label-principal Display Panel-0.2% (2.5 mL Container) (Olopatadine Fig1)
Label for Allwell eye allergy itch relief, olopatadine hydrochloride ophthalmic solution USP 0.2% (2 mg/mL), sterile solution in a 2.5 mL (0.085 FL OZ) bottle. The label includes usage instructions, storage temperature (2° to 25°C), tamper-evident warning, distributor Allwell Health Inc, Princeton, NJ, and states product is made in India.*
FDA Label Image

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

Package Label-principal Display Panel-0.2% (2.5 mL Container Carton) (Olopatadine Fig2)
Packaging label for Olopatadine Hydrochloride ophthalmic solution USP 0.2% by Allwell Health Inc. The 2.5 mL sterile eye drop solution provides original prescription strength antihistamine relief for eye allergy itch caused by pollen, pet dander, grass, and ragweed, for ages 2 and older. The label includes Drug Facts, directions for use, warnings, inactive ingredients, and tamper-evident information.*

* 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.