Calcium Carbonate
Calcium Carbonate is an FDA drug label for the active ingredient CALCIUM CARBONATE manufactured by Humco Holding Group, Inc. administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231215.
Generic: CALCIUM CARBONATE
Manufacturer: Humco Holding Group, Inc.
Product Type: HUMAN OTC DRUG
Route: ORAL
Dosage Form:
NDC: 0395-0431
Application: M001
Effective: 20231215
Active Ingredients: Active Ingredient Calcium Carbonate
Indications & Usage
Use For relief of heartburn, acid ingestion, and upset stomach associated with these symptoms.
Dosage & Administration
Directions Adults and children 6 yrs. of age and older: Take 1/2 level tsp. in 1/2 glass (4 fl oz) of water every 2 hrs. up to maximum dosage or as directed by a doctor.
Contraindications
Not available.
Warnings
Warnings Except under the supervision of a doctor: do not administer to children under 6 years of age. do not take more than 3 teaspoonfuls in a 24 hour period.
Adverse Reactions
Not available.
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