Systane Solution/ Drops
Product Images NDC 0065-0431

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Systane (NDC 0065-0431). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alcon Research Ltd, 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

Carton (Carton)

Systane lubricant eye drops packaging label featuring preservative-free vials. The box indicates the product contains polyethylene glycol and propylene glycol as active ingredients. It offers long-lasting relief and soothing comfort for dry eye therapy. The package contains 30 sterile vials, each with 0.7 mL solution. The labeler is Alcon Research Ltd, a Novartis company. The label includes a Drug Facts panel, directions for use, and manufacturer information.*

FDA Label Image

Cartonback

Drug Facts panel for Systane ophthalmic solution/drops with active ingredients polyethylene glycol 400 0.4% and propylene glycol 0.3% as lubricants. The panel includes uses for temporary relief of burning and irritation due to dryness of the eye, warnings for external use only, directions for applying 1 or 2 drops as needed, and other information such as storage at room temperature and protection from light. Inactive ingredients and contact information for questions are also provided.*

FDA Label Image

Cartonfront

Packaging label for Systane Original PF Lubricant Eye Drops, preservative-free for dry eye relief. The label highlights convenience of single vials for on-the-go use. It contains 30 sterile vials, each with 0.7 mL solution, for ophthalmic use. Manufactured by Alcon Laboratories, 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.