Up And Up Dual Action Acid Reducer Antacid Tablet, Chewable
Product Images NDC 82442-321

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Up And Up Dual Action Acid Reducer Antacid (NDC 82442-321). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Target Corporation, 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

Up And Up Dual Action Acid Reducer Antacid Container Image 1 Of 2 (Container Image 1 Of 2)

Up And Up Dual Action Acid Reducer Antacid Container Image 1 Of 2 (Container Image 1 Of 2)
Label for UP AND UP Dual Action Acid Reducer + Antacid chewable tablets containing famotidine 10 mg, calcium carbonate 800 mg, and magnesium hydroxide 165 mg. The label shows berry flavor, a depiction of a pink chewable tablet at actual size, and package count of 50 tablets. The product is made by Target Corporation and includes warnings, uses, directions, and storage information.*
FDA Label Image

Up And Up Dual Action Acid Reducer Antacid Container Image 2 Of 2 (Container Image 2 Of 2)

Up And Up Dual Action Acid Reducer Antacid Container Image 2 Of 2 (Container Image 2 Of 2)
Continuation of Drug Facts for UP AND UP DUAL ACTION ACID REDUCER ANTACID chewable tablets. This text panel lists inactive ingredients, including anhydrous lactose, artificial berry flavor, aspartame, various FD&C color additives, and other excipients. It also provides a contact number for questions or comments and notes distribution by Target Corporation, Minneapolis, MN.*

* 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.