Phospholine Iodide Kit
Product Images NDC 48102-053

4 FDA label images from Fera Pharmaceuticals, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Phospholine Iodide (NDC 48102-053). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fera Pharmaceuticals, Llc, 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

Structural Formula (Pho04 0000 01)

Structural Formula (Pho04 0000 01)
Chemical structure diagram of echothiophate iodide, the active ingredient in Phospholine Iodide ophthalmic solution. The structure shows ethyl groups, sulfur, nitrogen, and iodine atoms with detailed organic chemical bonds and molecular weight indicated.*
FDA Label Image

Figure (Pho04 0000 02)

Figure (Pho04 0000 02)
Packaging label for Phospholine Iodide (echothiophate iodide for ophthalmic solution) 0.125% (1/8%) 6.25 mg/5 mL ophthalmic solution kit by Fera Pharmaceuticals, LLC. The label includes usage instructions, storage conditions before and after reconstitution, barcode, and details about the sterile dropper and diluent ingredients.*
FDA Label Image

Figure (Pho04 0000 03)

Figure (Pho04 0000 03)
Phospholine Iodide 0.125% (6.25 mg/5 mL) ophthalmic solution label. The kit contains echothiophate iodide for ophthalmic use, prepared by CryoDesiccation and distributed by Fera Pharmaceuticals, LLC. The label includes storage instructions and a barcode, with a note to see accompanying literature for full details.*
FDA Label Image

Figure (Pho04 0000 04)

Figure (Pho04 0000 04)
Label for Phospholine Iodide sterile diluent for preparing ophthalmic solution. The product is a 5 mL (1/6 fl oz) eye drops vial by Fera Pharmaceuticals, LLC. Active ingredients and excipients are listed, including chlorobutanol, boric acid, and sodium phosphate, distributed by Mix Pharmaceutical, Locust Valley, NY. The label shows NDC 48102-055-05.*

* 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.