Uline Antacid
Product Images NDC 69790-089

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 Uline Antacid (NDC 69790-089). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Uline, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Uline Antacid 2 Rev 4 13 21 Label

Uline Antacid 2 Rev 4 13 21 Label
This is an antacid medication that contains Calcium Carbonate of 420mg per tablet. Users should not swallow the tablets whole. The medication is used to relieve symptoms related to heartburn, sour stomach, and acid indigestion. There are dosing instructions provided on the package depending on the age of the user and the severity of the symptoms, with a recommended limit of 2 tablets per 24-hour period. Users are advised to consult a doctor or pharmacist before usage, especially if pregnant, nursing, or have any underlying medical conditions. The medication also contains inactive ingredients such as sodium and cornstarch. If there are any questions or concerns, consumers can contact the manufacturer for more information.*
FDA Label Image

Uline Antacid Rev 4 13 21 Label

Uline Antacid Rev 4 13 21 Label
This is an antacid drug that contains Calcium Carbonate 420mg. It gives relief from the symptoms of acid indigestion, heartburn, and sour stomach. The drug is not to be used by pregnant or breastfeeding women and should be kept out of reach of children. If you want to use the drug, consult your doctor or pharmacist before you take it. The drug comes in tablets which should not be swallowed whole. The drug does not have significant information about directions except for how many times one should take the drug. The drug is manufactured by the Reorder No. 5-18596 company.*

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