Refresh Digital Solution/ Drops
Product Images NDC 0023-6952

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Refresh Digital (NDC 0023-6952). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Allergan, 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

Phone (Refresh Digital 01)

Refresh Digital 5 mg/mL ophthalmic solution/drops carton, featuring the proprietary name and active ingredients Carboxymethylcellulose sodium, Glycerin, and Polysorbate 80. The label shows a white and blue design with the Allergan, Inc. logo and the product NDC 0023-6952. The package indicates OTC human drug use for ophthalmic application.*

FDA Label Image

Principal Display Panelrefresh Digitalo.33 Fl Oz (10 mL) Sterile (Refresh Digital 02)

The packaging label for Refresh Digital Lubricant Eye Drops features a blue and white gradient background with yellow accents. The label highlights 10 mL sterile solution, with active ingredients Carboxymethylcellulose sodium 0.5%, Glycerin 1%, and Polysorbate 80 0.5%. The product is made by Allergan, Inc. and includes Drug Facts, directions, warnings, and other product details on the side panels.*

* 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.