Ursodiol
Product Images NDC 69189-0413

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ursodiol (NDC 69189-0413). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avera Mckennan Hospital, 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

Ursodiol-structure.jpg (21151543 F0bc 4bfd 9a78 86b1cc7987b0 01)

Chemical structure of Ursodiol, showing its molecular framework with hydroxyl groups and carboxyl functional group. This diagram illustrates the arrangement of atoms and bonds specific to Ursodiol, an active pharmaceutical ingredient.*

FDA Label Image

Figure-02.jpg (21151543 F0bc 4bfd 9a78 86b1cc7987b0 02)

The image shows a white plastic bottle with a child-resistant cap labeled Ursodiol. The label includes the product name Ursodiol and lists Avera McKennan Hospital as the labeler. The bottle appears to be a prescription medication container without visible dosage or strength information on the label face shown.*

FDA Label Image

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Ursodiol oral capsules packaging from Avera McKennan Hospital. The label shows the proprietary name Ursodiol and includes an image of a blister pack of capsules. The NDC 69189-0413 is associated with this product. The capsules are arranged in a rectangular blister card with a foil backing.*

FDA Label Image

Ursodiol 250 mg Tablet Label (6918904131)

Ursodiol 250 mg tablet label from Avera McKennan Hospital, Sioux Falls, SD. The label displays manufacturing and hospital lot numbers, an expiration date of 08/17/2016, and the NDC number 69189-0413. The label includes two barcodes and a small identifier code.*

* 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.