Refresh Optive Solution/ Drops
Product Images NDC 0023-3416

2 FDA label images from Allergan, Inc. · 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 (NDC 0023-3416). 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 Optive 01)

Phone (Refresh Optive 01)
Refresh Optive ophthalmic solution eye drops packaging label. The label shows the product name Refresh Optive with active ingredients Carboxymethylcellulose Sodium and Glycerin. The solution is indicated as a 5 mL bottle for ophthalmic use. The labeler is Allergan, Inc. The packaging background features blue and white colors with text and branding details.*
FDA Label Image

Principal Display Panelndc 0023-3416-30preservative-freerefreshoptive®lubricant Eye Dropsdual-action Relieffor Dry, Sensitive Eyes 30 Vials 0.01 Fl Oz (0.4 mL) Each Sterile (Refresh Optive 02)

Principal Display Panelndc 0023-3416-30preservative-freerefreshoptive®lubricant Eye Dropsdual-action Relieffor Dry, Sensitive Eyes 30 Vials 0.01 Fl Oz (0.4 mL) Each Sterile (Refresh Optive 02)
Packaging label for Refresh Optive Lubricant Eye Drops, preservative-free, containing Carboxymethylcellulose Sodium and Glycerin. The label highlights dual-action relief for dry, sensitive eyes in a solution/drops dosage form. The product comes in 30 sterile vials, each 0.4 mL, manufactured by Allergan, Inc., with instructions for use and drug facts including active ingredients 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.