Meijer Ultra Lubricant Eye Drops High Performance Solution/ Drops
Product Images NDC 41250-937

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Meijer Ultra Lubricant Eye Drops High Performance (NDC 41250-937). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meijer Distribution, 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

Meijer Ultra Lubricant Eye Drops 15ml Twin Pack (Kc Dl Meijer Ultra Lubricant Eye Drops Twin Pk)

Packaging label for Meijer Ultra Lubricant eye drops High Performance. The label shows the product name prominently with active ingredients Polyethylene glycol 400 at 0.4% and Propylene glycol at 0.3%. The label includes dosage form as ophthalmic solution drops in a total volume of 1 FL OZ (two 0.5 FL OZ bottles). The label also displays directions for use, warnings, inactive ingredients, and distributor information by Meijer Distribution, Inc. A barcode and tamper-evident warning are also visible.*

FDA Label Image

Meijer Ultra Lubricant Eye Drops 15ml (Kc Dl Meijer Ultra Lubricant Eye Drops)

Packaging label for Meijer Ultra Lubricant Eye Drops High Performance, an ophthalmic solution containing Polyethylene glycol 400 0.4% and Propylene glycol 0.3%. The label shows a 0.5 FL OZ (15 mL) bottle size, highlights 'Sterile' and 'High Performance Protection,' and includes a Drug Facts panel with active and inactive ingredients. Distributed by Meijer Distribution, Inc., Grand Rapids, MI.*

* 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.