Berkley And Jensen Lansoprazole Capsule, Delayed Release
Product Images NDC 68391-823

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Berkley And Jensen Lansoprazole (NDC 68391-823). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bjwc, 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

Berkley-jensen-lansoprazole-stretch-card-image-1.jpg (Berkley Jensen Lansoprazole Stretch Card Image 1)

Berkley-jensen-lansoprazole-stretch-card-image-1.jpg (Berkley Jensen Lansoprazole Stretch Card Image 1)
BERKLEY AND JENSEN LANSOPRAZOLE 15 mg delayed-release capsules label. The label highlights the product as an acid reducer for treating frequent heartburn with 24-hour effect. It indicates three 14-day courses of treatment with 3 bottles containing 14 capsules each, totaling 42 capsules. The label also shows an actual size image of the pink and gray capsule.*
FDA Label Image

Berkley-jensen-lansoprazole-stretch-card-image-2.jpg (Berkley Jensen Lansoprazole Stretch Card Image 2)

Berkley-jensen-lansoprazole-stretch-card-image-2.jpg (Berkley Jensen Lansoprazole Stretch Card Image 2)
Drug Facts panel for BERKLEY AND JENSEN LANSOPRAZOLE 15 mg delayed-release capsules. The label provides active ingredient, usage instructions for frequent heartburn, warnings including allergy and doctor consultation guidance, directions for 14-day treatment, information on inactive ingredients, and tips for managing heartburn. It also includes company contact info, gluten-free designation, package storage instructions, and a money-back guarantee statement from BJ's Wholesale Club.*

* 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.