Refresh Liquigel
Product Images NDC 0023-9205

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Refresh Liquigel (NDC 0023-9205). 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

Refresh Liquigel 1

REFRESH LIQUIGEL ophthalmic gel containing Carboxymethylcellulose sodium 10 mg/mL. The label features the product name prominently along with the active ingredient and strength. It is an over-the-counter human drug in gel form for ophthalmic use, labeled by Allergan, Inc. The NDC on the label is 0023-9205.*

FDA Label Image

Refresh Liquigel 2

Packaging label for REFRESH LIQUIGEL Lubricant Eye Gel, containing 10 mg/mL Carboxymethylcellulose sodium. It is a sterile 0.5 fl oz (15 mL) ophthalmic gel for eye lubrication. The label highlights its long-lasting relief for dry eyes and lists Allergan, Inc. as the labeler. The carton includes Drug Facts, directions, and warnings.*

* 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.