Cervidil Insert
Product Images NDC 55566-2800

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Cervidil (NDC 55566-2800). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ferring 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

Inner Carton Unit Carton

Inner Carton   Unit Carton
CERVIDIL 10 mg vaginal insert packaging label. The insert contains dinoprostone as the active ingredient. The label indicates it is for hospital use only, prescription only, and must be stored in a freezer between -30°C and -10°C. Labeler information is Ferring Pharmaceuticals Inc., and the NDC is 55566-2800. The packaging includes storage instructions and usage guidelines.*
FDA Label Image

Chemical Structure (Cervidil 01)

Chemical Structure (Cervidil 01)
An anatomical illustration showing a vaginal insert placed in the cervix. The image depicts the position of a vaginal drug insert used for controlled release, consistent with the application of a product like CERVIDIL (dinoprostone) vaginal insert.*
FDA Label Image

Principal Display Panel (10 mg Pouch Carton)

Principal Display Panel (10 mg Pouch Carton)
Diagram illustrating the components of a CERVIDIL insert, showing the vaginal insert with a labeled retrieval system and a dinoprostone slab.*
FDA Label Image

Cervidil 03

Cervidil 03
Chemical structure diagram of the active ingredient dinoprostone in CERVIDIL insert, showing its molecular components and bonds typically representing the prostaglandin E2 molecule.*

* 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.