Esomeprazole Magnesium Capsule, Delayed Release
Product Images NDC 21130-100

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Esomeprazole Magnesium (NDC 21130-100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Better Living Brands Llc, 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

Package Label-principal Display Panel (20 mg (14 Capsules Container Label))

FDA Label Image

Package Label-principal Display Panel (20 mg (14 Capsules Container Carton Label))

Package Label-principal Display Panel (20 mg (14 Capsules Container Carton Label))
This is a drug information document about a prescription drug (unnamed) with a 14-day treatment course, to treat frequent heartburn. The document includes instructions for use, dosage, precautions, and warnings. It should be kept away from children and not be taken for more than 14 days. Any rash, adverse reactions should be reported and medical advice should be sought. The drug is a delayed-release capsule with 20mg active ingredient Esomeprazole Magnesium USP. There are warnings about its usage in certain individuals and possible adverse symptoms. This is a USP approved drug with some side effects.*

* 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.