Gaviscon Tablet, Chewable
Product Images NDC 0135-0430

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Gaviscon (NDC 0135-0430). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Haleon Us Holdings 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

Gavison Extra Strength 100 Count Label (35d01fe6 542e 41fe A81b 49e1077a7e8e 01)

Packaging label of Gaviscon Extra Strength chewable tablets, showing the brand name prominently with a red banner for 'Extra Strength Antacid.' The label indicates 100 chewable tablets in original flavor and highlights fast-acting heartburn relief and acid control for hours. The product is labeled for oral use by Haleon US Holdings LLC.*

FDA Label Image

Gavison Extra Strength Cherry 100 Count Label (35d01fe6 542e 41fe A81b 49e1077a7e8e 02)

Gaviscon Extra Strength chewable tablets label showing brand name, antacid type, and cherry flavor. The package highlights fast-acting heartburn relief and acid control for hours. The label also shows a blue illustration of a human torso with a focus on the esophagus area, and states the contents include 100 chewable tablets. The manufacturer is Haleon US Holdings LLC.*

FDA Label Image

Gavison Regular Strength 100 Count Label (35d01fe6 542e 41fe A81b 49e1077a7e8e 03)

Gaviscon Regular Strength chewable tablets packaging featuring alumina and magnesium trisilicate as antacid ingredients. The label highlights relief for heartburn caused by acid reflux and a unique antacid barrier. It indicates the original flavor and a count of 100 chewable tablets.*

* 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.