Ultra Strength Antacid
Product Images NDC 68163-316

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ultra Strength Antacid (NDC 68163-316). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Raritan Pharmaceuticals 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

Drx Choice Ultra Strength Antacid 160 Chewable Tablets (102ab96pvlflb)

Drx Choice Ultra Strength Antacid 160 Chewable Tablets (102ab96pvlflb)
DR CHOICE is an antacid medication designed for fast relief of upset stomach, sour stomach, heartburn, and acid indigestion. The active ingredient per tablet is Calum Carbonate USP 1000mg. Users are advised to ask a doctor or pharmacist before use if they are currently taking prescription drugs since antacids may interact with certain prescription drugs. Adults and children 12 years of age and over must chew two to three tablets completely as symptoms occur or as directed by a doctor, without swallowing tablets whole. The maximum dosage must not exceed seven tablets in 24 hours. Users are advised not to use the maximum dosage of DR CHOICE for more than two weeks except under the advice and supervision of a doctor. This product is manufactured by Raritan Pharmaceuticals and contains some inactive ingredients such as adipic acid, D&C Red No. 27 Lake, DEC Yellow 10 Lake, Getrose, FDEC Blue No. 1 Lake, FOAC Yelow No. 6 Lake, flavor, magnesium stearate, maltodextrin, starch, and sucralose. The product is gluten-free, not distributed by GlaxoSmithKine LLC, and is available to consumers.*
FDA Label Image

Drx Choice Ultra Strength Antacid 72 Chewable Tablets (103af72dclflb.tums 011521.jpg)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.