Prednisolone Acetate Suspension/ Drops
Product Images NDC 50090-1912

2 FDA label images from A-s Medication Solutions · 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 Prednisolone Acetate (NDC 50090-1912). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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

Label Image (Lbl500901912)

Label Image (Lbl500901912)
Label for PREDNISOLONE ACETATE 10 mg/mL ophthalmic suspension/drops, a prescription drug by A-S Medication Solutions. The label shows the product number 4293-0 and a lot number. It includes storage instructions to keep at 77 degrees Fahrenheit, protect from freezing, and store upright. The container size is 10 mL.*
FDA Label Image

The Following Structure For Prednisolone Acetate Ophthalmic Suspension, Usp 1% Is A Sterile, Topical Anti-inflammatory Agent For Ophthalmic Use. Its Chemical Name Is 11ß,17, 21-trihydroxypregna-1,4-diene-3, 20-dione 21-acetate. (Prednisolone Acetate 01)

The Following Structure For Prednisolone Acetate Ophthalmic Suspension, Usp 1% Is A Sterile, Topical Anti-inflammatory Agent For Ophthalmic Use.  Its Chemical Name Is 11ß,17, 21-trihydroxypregna-1,4-diene-3, 20-dione 21-acetate. (Prednisolone Acetate 01)
Chemical structure diagram of prednisolone acetate, showing the arrangement of carbon rings and functional groups including hydroxyl and acetate groups, consistent with the corticosteroid structure.*

* 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.