Acydone
Product Images NDC 84831-005

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Acydone (NDC 84831-005). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sigma, 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

Interior Leaflet (3.9.1 Leaflet.pdf)

Interior Leaflet (3.9.1 Leaflet.pdf)
Drug facts text panel for Acydone Gel, a suspension containing aluminum hydroxide, magnesium hydroxide, and simethicone. The panel includes composition details, dosage instructions for adults, indications, contraindications, precautions, side effects, drug interactions, overdose information, storage instructions, and manufacturer information from Sigma.*
FDA Label Image

Box Full (3.9.2 Cases And Labels.pdf (1))

Box Full (3.9.2 Cases And Labels.pdf (1))
Label for Acydone Gel, an oral suspension containing aluminum hydroxide, magnesium hydroxide, and simethicone as active ingredients. The label shows the Sigma Corp. logo and states the product is an antacid and antiflatulent. The package size is 100 ml, with instructions and pharmaceutical information included. The labeler is Sigma.*
FDA Label Image

Label Front (3.9.2 Cases And Labels.pdf)

Label Front (3.9.2 Cases And Labels.pdf)
Label for Acydone Gel suspension, featuring active ingredients aluminum hydroxide 200 mg, magnesium hydroxide 200 mg, and simethicone 25 mg per 5 ml. Contains sorbitol and includes directions to shake well before use. Suspension form, 100 ml size, for oral administration. Labeler: Industria Sigma Quimico Farmaceutica.*

* 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.