Refresh Optive Advanced Solution/ Drops
Product Images NDC 0023-4491

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 Refresh Optive Advanced (NDC 0023-4491). 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 Optive Advanced 1

Refresh Optive Advanced 1
REFRESH OPTIVE Advanced ophthalmic solution/drops packaging label. The label displays the proprietary name "REFRESH OPTIVE Advanced," indicating a multi-ingredient formulation including carboxymethylcellulose sodium, glycerin, and polysorbate 80. The labeler is Allergan, Inc. The label includes product information in English and Spanish, and the product NDC is 0023-4491.*
FDA Label Image

Refresh Optive Advanced 2

Refresh Optive Advanced 2
Packaging label for REFRESH Optive Advanced Lubricant Eye Drops, a sterile ophthalmic solution indicated for dry eye relief. The label states it contains 30 single-use containers, each with 0.01 fl oz (0.4 mL). The product is preservative-free with triple-action relief, containing carboxymethylcellulose sodium, glycerin, and polysorbate 80. Manufactured by Allergan, Inc.*

* 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.