Tums
calcium carbonate · Tablet, Chewable · Oral
Active ingredient
Active ingredient (per tablet) Calcium carbonate 750 mg
Purpose
Purpose Antacid
Uses
Uses relieves heartburn acid indigestion sour stomach upset stomach associated with these symptoms
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.
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.
When using this product
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
Keep out of reach of children.
Directions
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
Inactive ingredients
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
Label text from the FDA structured product label by Haleon US Holdings LLC (revised Sep 4, 2026). Long sections are shortened; the complete label is on DailyMed.
Active ingredients
- Calcium Carbonate in 36 products
Tums NDC products (36)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 0135-0623 | Calcium Carbonate 750 mg/1 Tablet, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0456 | Calcium Carbonate 750 mg/1 Tablet, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0521 | Calcium Carbonate 750 mg/1 Tablet | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0540 | Calcium Carbonate 1000 mg/1 Tablet, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0553 | Calcium Carbonate 1000 mg/1 Tablet, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0560 | Calcium Carbonate 1177 mg/1 Bar, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0561 | Calcium Carbonate 1177 mg/1 Bar, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0569 | Calcium Carbonate 1177 mg/1 Bar, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0611 | Calcium Carbonate 500 mg/1 Tablet, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0246 | Calcium Carbonate 750 mg/1 Tablet, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-1000 | Calcium Carbonate 750 mg/1 Tablet | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-1001 | Calcium Carbonate 750 mg/1 Tablet | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-1002 | Calcium Carbonate 750 mg/1 Tablet, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-1326 | Calcium Carbonate 1000 mg/1 Tablet, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-1327 | Calcium Carbonate 750 mg/1 Tablet, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-1328 | Calcium Carbonate 1000 mg/1 Tablet, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-5970 | Calcium Carbonate 750 mg/1 Tablet, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-5971 | Calcium Carbonate 750 mg/1 Tablet, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0180 | Calcium Carbonate 1000 mg/1 Tablet, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0071 | Calcium Carbonate 500 mg/1 Tablet | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0074 | Calcium Carbonate 750 mg/1 Tablet | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0076 | Calcium Carbonate 750 mg/1 Tablet | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0118 | Calcium Carbonate 1000 mg/1 Tablet, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0140 | Calcium Carbonate 750 mg/1 Tablet | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0154 | Calcium Carbonate 750 mg/1 Tablet | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0155 | Calcium Carbonate 750 mg/1 Tablet, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0178 | Calcium Carbonate 750 mg/1 Tablet | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0070 | Calcium Carbonate 500 mg/1 Tablet | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0181 | Calcium Carbonate 1000 mg/1 Tablet, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0188 | Calcium Carbonate 750 mg/1 Tablet, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0221 | Calcium Carbonate 750 mg/1 Tablet, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0227 | Calcium Carbonate 750 mg/1 Tablet, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0228 | Calcium Carbonate 1000 mg/1 Tablet, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0235 | Calcium Carbonate 1000 mg/1 Tablet, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0243 | Calcium Carbonate 750 mg/1 Tablet, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
| 0135-0245 | Calcium Carbonate 750 mg/1 Tablet, Chewable | Haleon US Holdings LLC | OTC MONOGRAPH DRUG |
Tums recalls
- D-0073-2024 Nov 8, 2023 · Class II · Completed
Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool. - D-0074-2024 Nov 8, 2023 · Class II · Completed
Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool. - D-0075-2024 Nov 8, 2023 · Class II · Completed
Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool. - D-0079-2024 Nov 8, 2023 · Class II · Completed
Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool. - D-850-2013 Aug 14, 2013 · Class III · Terminated
Presence of Foreign Tablets/Capsules: Product labeled TUMS Ultra Assorted Berries 1000mg Chewable tables, may contain EX TUMS Assorted Berries 750mg tablets
Frequently asked questions
What is Tums used for?
Uses relieves heartburn acid indigestion sour stomach upset stomach associated with these symptoms
Who makes Tums?
Tums is listed by 1 labeler in the FDA NDC directory, including Haleon US Holdings LLC.
Has Tums been recalled?
The FDA enforcement database lists 5 recalls for Tums, most recently D-0073-2024 (class ii): Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool.