Active Ingredient (In Each Tablet)
Calcium carbonate 500 mg
Sunmark Calcium Antacid
FDA Label NDC 49348-958
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Mckesson for the product Sunmark Calcium Antacid (NDC 49348-958). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient (in each tablet), purpose, uses, warnings, ask a doctor or pharmacist before use if you are, when using this product, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antacid
Uses
relieves
- acid indigestion
- heartburn
Warnings
Ask A Doctor Or Pharmacist Before Use If You Are
taking a prescription drug. Antacids may interact with certain prescriptiom drugs.
When Using This Product
do not take more than 16 tablets in a 24-hour period, or use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor.
Keep Out Of Reach Of Children
Directions
- chew 2-4 tablets as symptoms occur, or as directed by a doctor
Other Information
- do not use if seal under cap is torn or missing
- store at room temperature
Inactive Ingredients
adipic acid, corn starch, crospovidone, D and C red 27 lake, D and C red 30 lake, D and C Yellow 10 lake, dextrose, FD and C blue 1 lake, FD and C yellow 6 lake, flavors, magnesium stearate, maltodextrin, sucrose, talc
Principal Display Panel
Sunmark
compare to Tums active ingredient
calcium antacid
regular strength
fast relief of heartburn and acid indigestion
daily source of calcium
assorted fruit flavors
150 chewable tablets
Label (126af)
* Please review the disclaimer below.
