Omeprazole Tablet, Delayed Release
Product Images NDC 69230-318

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Omeprazole (NDC 69230-318). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Camber Consumer Care 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.

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FDA Label Image

Omecarton (Omecarton)

Omecarton (Omecarton)
Sorpay Omeprazole is an Acid Reducer that treats Frequent Heartburn occurring 2 or more days a week. One 14-day course of treatment is required. Each tablet of this delayed-release medication contains 20mg of active ingredient, Omeprazole Magnesium USP, which reduces acid in the stomach. Not recommended for people with certain conditions such as trouble or pain swallowing food, vomiting with blood, or black stools, heartburn with dizziness and sweating, frequent chest pain, weight loss, or nausea. This medication can interact with certain prescription drugs and cause a rash or joint pain. Children under 18 need a doctor's recommendation. The tablet should not be crushed or chewed and one per day should be taken with water before breakfast. For more information, consumers can call a customer care service.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.