Freshkote Preservative Free Lubricating Eye Drops
Product Images NDC 15821-108

2 FDA label images from Focus Laboratories, 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 Freshkote Preservative Free Lubricating Eye Drops (NDC 15821-108). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Focus Laboratories, 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

Image Description (Freshkote Mdu Box Label)

Image Description (Freshkote Mdu Box Label)
Packaging label for FreshKote Preservative Free Lubricating Eye Drops by FOCUS Laboratories, Inc. The label highlights active ingredients polyvinyl alcohol 2.7% and povidone 2.0%, indicating its use as a lubricant for dry eye symptoms. The 0.33 fl oz (10 mL) product is described as preservative-free and suitable for contact lens users. Directions, warnings, and inactive ingredient details are included, along with manufacturer contact information and a barcode.*
FDA Label Image

Image Description (Freshkote Mdu Container Label)

Image Description (Freshkote Mdu Container Label)
Label for FreshKote Preservative Free Lubricating Eye Drops by FOCUS Laboratories, Inc. The label shows dosage directions to instill 1 or 2 drops in the affected eye(s) as needed. It lists active ingredients including Polyvinyl alcohol 2.7% and Povidone 2.0%, and emphasizes the product is for external use only. The sterile product volume is 0.33 fluid ounces (10 mL). Storage instructions state to keep at 20-25°C (68-77°F) and not to use if the seal is damaged.*

* 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.