Rugby Lubricant Eye Drops Solution/ Drops
Product Images NDC 0536-1387

View Photos of 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 Rugby Lubricant Eye Drops (NDC 0536-1387). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rugby Laboratories, 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

Rugby Lubricant Eye Drops 30ct (Rugby Lubricant Eye Drops 30ct)

Rugby Lubricant Eye Drops 30ct (Rugby Lubricant Eye Drops 30ct)
Packaging label for Rugby Lubricant Eye Drops containing Carboxymethylcellulose Sodium 0.5% as the active ingredient. The product is preservative-free and supplied in 30 single-use containers of 0.01 FL OZ (0.4 mL) each. The label includes usage instructions, warnings, inactive ingredients, and contact information for Rugby Laboratories, the distributor. The packaging highlights that the drops provide immediate, long-lasting relief for dry, irritated eyes.*
FDA Label Image

Rugby Lubricant Eye Drops 50ct (Rugby Lubricant Eye Drops 50ct)

Rugby Lubricant Eye Drops 50ct (Rugby Lubricant Eye Drops 50ct)
The packaging label for Rugby Lubricant Eye Drops features the product name with Carboxymethylcellulose Sodium 0.5% as the active ingredient. It highlights the product as preservative-free and provides 50 single-use containers, each containing 0.01 FL OZ (0.4 mL). The label includes usage instructions, drug facts, warnings, storage information, and distributor details from Rugby Laboratories.*

* 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.