Acid Reducer Tablet, Delayed Release
Product Images NDC 69618-054

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 Acid Reducer (NDC 69618-054). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Reliable 1 Laboratories 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 Tablet Bottle))

Package Label-principal Display Panel (20 mg (14 Tablet Bottle))
Acid Reducer Omeprazole 20 mg delayed-release tablets label from Reliable-1 Laboratories LLC. The label includes dosage information, a 14-tablet count, and directions for use. It advises a 14-day course of treatment and includes warnings and storage instructions. The label is divided into top, back, and bottom plies with detailed usage and ingredient information.*
FDA Label Image

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

Package Label-principal Display Panel (20 mg Container Carton Label)
The packaging label for Acid Reducer Omeprazole delayed-release tablets, 20 mg, by Reliable 1 Laboratories LLC. The label includes product name, strength, dosage form, and package size: 42 tablets for three 14-day treatment courses. The carton is primarily purple with white and blue text, featuring Drug Facts panels, dosing instructions, warnings, and a barcode. The labeler address and a note about the product origin are also visible.*

* 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.