Calcium Carbonate Suspension
Product Images NDC 0121-0766

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Calcium Carbonate (NDC 0121-0766). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pai Holdings, Llc Dba Pai Pharma, 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

Calcium 01

Label of Quality Value Calcium Carbonate Oral Suspension 1250 mg/5 mL antacid by PAI Pharmaceutical Associates, Inc. This 16 fl oz (473 mL) oral suspension is sugar-free, alcohol-free, and sodium-free. The label includes drug facts, usage, warnings, directions, inactive ingredients, and contact information for questions.*

FDA Label Image

Calcium 02

Calcium Carbonate Oral Suspension maximum strength, 1250 mg/5 mL (equivalent to 500 mg elemental calcium) in a 5 mL unit-dose cup format. The label includes sugar-free, alcohol-free, and sodium-free claims, states it is an antacid requiring shaking before use, and is manufactured by PAI Holdings, LLC dba PAI Pharma in Greenville, SC. The packaging features directions, warnings, ingredient list, and other product information.*

* 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.