Calmicid Ac Tablet, Coated
Product Images NDC 54473-411

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 Calmicid Ac (NDC 54473-411). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Melaleuca, 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

369d7d65 9f92 F138 E063 6294a90a0312

369d7d65 9f92 F138 E063 6294a90a0312
Label detail from Calmicid AC Acid Reducer 20 mg coated tablets packaging showing an illustration of a single white coated tablet with the text 'actual size' and the quantity statement '50 Tablets' on a blue background.*
FDA Label Image

Calmicid Box.jpg (Calmicid Box)

Calmicid Box.jpg (Calmicid Box)
Packaging label for Calmicid AC Acid Reducer Famotidine Tablets USP 20 mg, 50 coated tablets by Melaleuca, Inc. The label highlights use for heartburn and acid indigestion relief, includes drug facts with active ingredient, warnings, directions, inactive ingredients, and contact information. The label shows a white bottle image with purple and orange accents and includes a barcode.*
FDA Label Image

Calmicid Bottle.jpg (Calmicid Bottle)

Calmicid Bottle.jpg (Calmicid Bottle)
The image shows a white plastic bottle with a purple and white label for Calmicid AC Acid Reducer tablets. The label states the product contains Famotidine 20 mg tablets, is maximum strength, and is used to prevent and relieve heartburn due to acid indigestion. The bottle contains 50 coated oral tablets and is labeled by Melaleuca, Inc. Warnings about proper use and new warnings are also visible.*

* 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.