Genexa Antacid
Product Images NDC 69676-0057

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 69676-0057). 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

Label R-20210128 (back) (Label R 20210128 (back))

Label R-20210128 (back) (Label R 20210128 (back))
Drug Facts panel for Genexa Antacid Maximum Strength tablets with active ingredient calcium carbonate USP 1000 mg as an antacid. The label includes uses for heartburn, acid indigestion, sour stomach, and related symptoms. Warnings advise consulting a doctor if taking prescription drugs, dosage limits, and keeping out of reach of children. Directions indicate adults and children 12 years and older should chew 2-3 tablets as needed. Other information covers elemental calcium content and storage conditions. Lists inactive ingredients including organic beet root and carnauba wax, and provides contact information and manufacturer details.*
FDA Label Image

Label R-20210128 (front) (Label R 20210128 (front))

Label R-20210128 (front) (Label R 20210128 (front))
Label of Genexa Antacid Maximum Strength chewable tablets by Genexa Inc. The label highlights relief for heartburn, acid indigestion, and upset stomach, with 1000 mg of calcium carbonate per tablet. The product contains 72 chewable tablets and features organic berry and vanilla flavor. It is marked Non-GMO Project Verified with no common allergens, artificial dyes, or talc.*

* 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.