Dry Eye Relief Gel
Product Images NDC 70000-0088

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Dry Eye Relief (NDC 70000-0088). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cardinal Health 110, Llc. Dba Leader, 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

1 (1)

Label for Dry Eye Relief ophthalmic gel containing polyethylene glycol 400 0.4% and propylene glycol 0.3%. The label indicates sterile gel in a 0.33 fluid ounce (10 mL) container. It includes directions for use, warnings, manufacturer information for Cardinal Health 110, LLC DBA Leader, a tamper seal advisory, and a 100% money-back guarantee statement. The label is primarily red, green, and white with detailed product and regulatory text.*

FDA Label Image

2 (2)

Packaging label for Dry Eye Relief ophthalmic gel by Leader, containing polyethylene glycol 400 0.4% and propylene glycol 0.3% as lubricants. The label shows a 0.33 FL OZ (10 mL) bottle size and highlights moisturizing dry eyes. Includes Drug Facts, warnings, directions, inactive ingredients, and a 100% Money Back Guarantee. Distributed by Cardinal Health 110, LLC.*

* 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.