Exovisse Preservative-free Artificial Tears Liquid
Product Images NDC 87106-005

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 Exovisse Preservative-free Artificial Tears (NDC 87106-005). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Yd Bio Usa, 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

Carton (0 5 mL Exovisse Carton)

Carton (0 5 mL Exovisse Carton)
Exovisse Preservative-Free Artificial Tears Lubricant Eye Gel Drops packaging label. The label shows the product as a sterile ophthalmic liquid with a strength of 0.2 g/100 mL, indicated for mild to moderate dry eye symptoms. It highlights features such as stabilizing tear film, reducing tear evaporation, and suitability for contact lens wearers. The label also includes directions, active and inactive ingredients, manufacturer YD BIOPHARMA, contact information, and a barcode. The package dimensions are marked in millimeters.*
FDA Label Image

Label (0 5 mL Exovisse Label)

Label (0 5 mL Exovisse Label)
Label for Exovisse Preservative-Free Artificial Tears Lubricant Eye Gel Drops by YD BIO USA, INC. The label highlights the product as preservative-free, sterile, and suitable for mild to moderate dry eye symptoms. The liquid ophthalmic gel drops come in a .2 g/100 mL strength, with a package size of 0.013 FL OZ (0.5 mL). Manufacturer and distribution information is provided along with usage 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.