Archies Dry Eye Relief Solution/ Drops
Product Images NDC 83737-001

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Archies Dry Eye Relief (NDC 83737-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Archie's Remedies, 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

Archie's Dry Eye Relief 30ct (Archies Dry Eye Relief 30ct)

Packaging label for Archies Dry Eye Relief Ultra Formula ophthalmic solution/drops. The label shows the product as preservative and paraben-free eye drop lubricant containing 30 single-use vials. It includes active ingredients polyethylene glycol 400 (0.4%) and propylene glycol (0.3%) with directions for use and warnings. The labeler is Archie's Remedies, distributed by KC Pharmaceuticals, Pomona, CA.*

FDA Label Image

Archie's Dry Eye Relief 60ct (Archies Dry Eye Relief 60ct)

Archies Dry Eye Relief Ultra Formula ophthalmic solution/drops packaging label featuring preservative- and paraben-free eye drop lubricant in 60 single-use vials. The label highlights active ingredients polyethylene glycol 400 0.4% and propylene glycol 0.3%, with detailed drug facts and usage directions. The product is distributed by Archie's Remedies and includes branding and illustrations emphasizing the product's soothing, long-lasting eye relief properties.*

* 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.