Active Ingredient(S)
Calcium carbonate USP 500mg
Calcium Carbonate Tablet, Chewable
FDA Label NDC 69168-124
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Allegiant Health for the product Calcium Carbonate (NDC 69168-124). 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(s), purpose, use(s), ask a doctor before use if you, when using this product, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antacid
Use(S)
relieves
- heartburn
- sour stomach
- acid indigestion
- upset stomach associated with these symptoms
Ask A Doctor Before Use If You
- kidney disease
- taking any prescription drugs; antacids may interact with certain prescription drugs
When Using This Product
do not take more than 15 tablets in a 24 our period or use the maximum dosage of this product
for more than 2 weeks.
Directions
chew 2-4 tablets as symptoms occur, repeat hourly if needed
Other Information
- Calcium content per tablets: 200mg
- store at 15°-30°C (59°-86°F)
- do not use if imprinted safety seal under cap is broken or
missing
Inactive Ingredients
FD&C yellow #6 aluminum lake, magnesium stearate, maltodextrin, orange flavor, sorbitol
Questions/Comments
Call 1-888-952-0050
(Monday-Friday 9 AM – 5 PM EST)
Principal Display Panel
Calcium Carbonate 500mg
* Please review the disclaimer below.
