Dry Eye Relief Gel
Product Images NDC 70000-0089

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Dry Eye Relief (NDC 70000-0089). 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)

The label for Dry Eye Relief ophthalmic gel, containing Carboxymethylcellulose sodium 10 mg/mL (1%) as the active ingredient. The label states the product is sterile, with a volume of 0.5 FL OZ (15 mL). It includes usage warnings, directions for instilling 1 or 2 drops in the affected eye(s), and storage information. The labeler is Cardinal Health 110, LLC. DBA Leader, with contact information and manufacturing details listed. The label also notes a 100% money-back guarantee and tamper-evident instructions.*

FDA Label Image

2 (2)

Packaging label for Dry Eye Relief Carboxymethylcellulose Sodium 1% eye lubricant gel by Cardinal Health 110, LLC. The label shows the product name, active ingredient, strength, and volume (0.5 FL OZ/15 mL). It includes drug facts with active and inactive ingredients, uses, warnings, directions, and storage information. The label compares this product to Refresh Liquigel lubricant eye gel and features a tamper-evident caution and a 100% money-back guarantee.*

* 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.