Bonjesta Tablet, Extended Release
Product Images NDC 55494-120

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Bonjesta (NDC 55494-120). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Duchesnay Usa, 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

Bottle Label-outside Front Cover With Imprint Area For Lot & Expiry (Bottle Label 1)

Bottle Label-outside Front Cover With Imprint Area For Lot & Expiry (Bottle Label 1)
This is a description of a medication called "Bonjesta". It comes in extended-release tablets that contain 20mg of Doxylamine succinate and pyridoxine hydrochloride each. Patients are instructed to swallow the tablet whole, and it should be stored between 20°C to 25°C (68°F to 77°F). The medication is prescribed by a doctor or pharmacist and comes with a patient package insert. The manufacturer is located in Pennsylvania, USA.*
FDA Label Image

Bottle Label – Inside Cover (Bottle Label Inside)

Bottle Label – Inside Cover (Bottle Label Inside)
Bonjesta is a medication containing doxylamine succinate and pyridoxine hydrochloride and is available as extended-release tablets. It is important to swallow the tablets whole and not crush, chew, or split them. One package contains 60 extended-release tablets. This medication is used for morning sickness in pregnant women. The usual dosage is not provided in the text. The remaining text appears to be illegible.*
FDA Label Image

Halal Symbol (Halal)

FDA Label Image

Kosher Symbol (Kosher)

FDA Label Image

Structure-1 (Structure 1)

FDA Label Image

Structure-2 (Structure 2)

* 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.