Genexa Antacid Tablet, Chewable
Product Images NDC 69676-0072

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 Genexa Antacid (NDC 69676-0072). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Genexa 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

16a Antacid Back 2022-01-13 (16a Antacid Back 2022 01 13)

16a Antacid Back 2022-01-13 (16a Antacid Back 2022 01 13)
Drug Facts panel for Genexa Antacid Maximum Strength chewable tablets, containing 1000 mg of calcium carbonate per tablet as the active ingredient. The panel includes indications for relief of heartburn, acid indigestion, and sour or upset stomach, warnings about use limits and interactions, directions for adults and children 12 years and older, and other information such as elemental calcium content and storage instructions. Inactive ingredients and a contact phone number are also listed.*
FDA Label Image

16a Antacid Pdp 2022-01-13 (16a Antacid Pdp 2022 01 13)

16a Antacid Pdp 2022-01-13 (16a Antacid Pdp 2022 01 13)
Label for Genexa Antacid Maximum Strength chewable tablets containing 1000 mg calcium carbonate. The label highlights relief for heartburn, acid indigestion, and upset stomach. It states the product is made without talc, FD&C blue no. 1 lake, FD&C red no. 40 lake, sucrose, and more. The flavor is Organic Berry & Vanilla, and the package contains 72 chewable tablets. Non-GMO Project Verified seal is present.*

* 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.