Prednisolone Acetate
Product Images NDC 67296-0872

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Prednisolone Acetate (NDC 67296-0872). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

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- (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- (Prednisolone Acetate 01)
Chemical structure of Prednisolone Acetate, showing its steroid backbone with hydroxyl, acetyl, and ketone functional groups. The structure includes multiple rings and side chains characteristic of corticosteroids.*
FDA Label Image

Pacific Pharma (Prednisolone Acetate 02)

FDA Label Image

Ndc 60758-119-10prednisolone Acetateophthalmic Suspension, Usp 1%10 mLsterilerx Only (Prednisolone Acetate 03)

Ndc 60758-119-10prednisolone Acetateophthalmic Suspension, Usp 1%10 mLsterilerx Only (Prednisolone Acetate 03)
Label for PREDNISOLONE ACETATE ophthalmic suspension USP 1%, 10 mL sterile bottle by Pacific Pharma. The label includes product concentration, volume, sterility, and Rx only designation. Additional text details preservatives, inactive ingredients, storage instructions, and usage notes. Distributed for Allergan USA, Inc.*

* 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.