Prednisolone Acetate Suspension/ Drops
Product Images NDC 68071-2222

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Prednisolone Acetate (NDC 68071-2222). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare Pharmaceuticals,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

Pdp (68071 2222 5)

Pdp (68071 2222 5)
Care Pharmaceuticals, Inc. offers Prednisolone Acetate 1% ophthalmic suspension in a 5mL bottle. The product contains a warning to keep it out of reach of children and store it at a controlled temperature of 68-77°F. The bottle includes the lot number (000000) and the expiration date (00-00) as well as the product number (R0589005) and instructions to consult a doctor for medical advice about side effects, which can also be reported to the FDA. The manufacturer's label provides a full list of ingredients.*
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)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.