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OTC products · Product label record

Tums Chewy Bites Wintermint and Vanilla Cream drug information

CALCIUM CARBONATE
Haleon US Holdings LLC · ORAL

Product NDC: 0135-5971

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameCALCIUM CARBONATE
Labeler / manufacturerHaleon US Holdings LLC
RouteORAL
Drug classDrug class not supplied in source label
Product NDC0135-5971
Label effective date2026-09-04

Official product label reference

Tums Chewy Bites Wintermint and Vanilla Cream — Haleon US Holdings LLC

This page contains 11 source sections for CALCIUM CARBONATE, oral route. Label set 4f094feb-8de1-4ccb-e063-6294a90acec2, version 2.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Uses relieves heartburn acid indigestion sour stomach upset stomach associated with these symptoms

Purpose

Purpose Antacid
Dosage and administration — label text
Directions adults and children 12 years of age and over: chew 2-4 tablets as symptoms occur, or as directed by a doctor. Chew or crush tablets completely before swallowing. do not take for symptoms that persist for more than 2 weeks unless advised by a doctor
Warnings
Warnings Ask a doctor or pharmacist before use if you are presently taking a prescription drug. Antacids may interact with certain prescription drugs. When using this product do not take more than 6 tablets in 24 hours if pregnant do not take more than 6 tablets in 24 hours do not use the maximum dosage for more than 2 weeks, except under the advice and supervision of a doctor Keep out of reach of children.
Active ingredient
Active ingredient (per tablet) Calcium carbonate 750 mg
Ask a doctor or pharmacist
Ask a doctor or pharmacist before use if you are presently taking a prescription drug. Antacids may interact with certain prescription drugs.
While using this medicine
When using this product do not take more than 6 tablets in 24 hours if pregnant do not take more than 6 tablets in 24 hours do not use the maximum dosage for more than 2 weeks, except under the advice and supervision of a doctor
Child safety
Keep out of reach of children.
Unclassified section
Other information each chewable tablet contains: elemental calcium 300 mg do not store above 25°C (77°F) contains FD&C Yellow No. 5 (tartrazine) as a color additive Additional Information Do not use if printed inner safety seal under cap is broken or missing.
Inactive ingredient
Inactive ingredients acacia gum, beeswax, carnauba wax, citric acid, coconut oil, corn starch, corn syrup, dextrin, FD&C blue no.1 aluminum lake, FD&C red no. 40, FD&C red no. 40 aluminum lake, FD&C yellow no. 5 aluminum lake (tartrazine), maltodextrin, monoammoniated glycyrrhizin, natural and artificial flavors, pharmaceutical ink, phosphoric acid, povidone, propylene glycol, purified water, shellac, sodium benzoate, sorbic acid, sorbitol, soy lecithin, sucrose, titanium dioxide, vegetable oil
Questions
Questions or comments? 1-800-452-0051

Official sources and product identifiers

Substances listed: CALCIUM CARBONATE

RxNorm identifiers: 308915, 1044532

Package NDC codes

0135-5971-01

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.