Ko-lanta Suspension
Product Images NDC 57896-004

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Ko-lanta (NDC 57896-004). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Geri-care Pharmaceuticals, Corp, 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

1 (Adw629)

Label for KO-LANTA oral suspension, a human OTC drug containing aluminum hydroxide 200 mg, magnesium hydroxide 200 mg, and simethicone 20 mg per 5 mL. The label states it is an antacid/anti-gas product for acid indigestion, sour stomach, heartburn, and gas relief. The 12 fl oz (355 mL) bottle is kosher for Passover and contains 0.15% alcohol. Distributed by ADWE Laboratories, Brooklyn, NY.*

* 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.