Pred Forte Suspension/ Drops
Product Images NDC 11980-180

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Pred Forte (NDC 11980-180). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Allergan, 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

Pred Forte 01

Pred Forte 01
Chemical structure diagram of prednisolone acetate showing its molecular framework, as identified by the label.*
FDA Label Image

Pred Forte 02

FDA Label Image

Pred Forte 03

Pred Forte 03
Label for PRED FORTE (prednisolone acetate) ophthalmic suspension, USP 1%, sterile, in a 5 mL bottle. The label shows the Allergan logo, product name, active ingredient concentration, and volume. It includes storage instructions, a barcode, and a list of inactive ingredients, as well as directions to shake well before use.*
FDA Label Image

Pred Forte 04

Pred Forte 04
Packaging label for PRED FORTE 1% prednisolone acetate ophthalmic suspension, USP sterile, 10 mL by Allergan, Inc. The label includes active and inactive ingredients, storage instructions, and dosage directions. The product is noted as Rx only with NDC 11980-180-10 and is produced in France.*
FDA Label Image

Pred Forte 05

Pred Forte 05
Carton packaging for PRED FORTE 1% prednisolone acetate ophthalmic suspension, 15 mL, manufactured by Allergan, Inc. The label contains information including active ingredients, preservatives, inactives, storage instructions, and usage directions. The packaging is primarily purplish-pink and black with white text and includes a barcode and product lot/expiration details.*

* 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.