TUMS
- Product NDC
- 0135-0243
- 11-digit product format
- 001350243
- Labeler code
- 0135
- Product ID
- 0135-0243_4e6d1e5b-2025-907d-e063-6294a90abe8c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- calcium carbonate
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Haleon US Holdings LLC
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2010-03-24
- Substance
- CALCIUM CARBONATE
- Active strength
- 750 mg/1
- Pharmacologic classes
- Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2022-08-30 03:57 UTC · source 2022-08-29 | excluded product | product | 0135-0243 | I | Inactivated by FDA | excluded / ndc_excluded.zip | fb8cb913e6d1… | eb8c232b6be0… | ||
| 2022-08-30 03:57 UTC · source 2022-08-29 | excluded package | package | 0135-0243 | 0135-0243-02 | I | Inactivated by FDA | excluded / ndc_excluded.zip | fb8cb913e6d1… | eb8c232b6be0… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- TUMS
- Brand name suffix
- Smoothies
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| CALCIUM CARBONATE | 750 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| H0G9379FGK | Internal UNII lookup |
Harmonized RxCUI identifiers#
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| c22944b8-8733-4689-be0c-f320467f79ea | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| bee4fa8d-8d82-423a-a0b5-40a89dd13a99 | Product name | 1 | 20250618 |
| e0d2eb29-08bd-4bba-90d1-c91c68a38767 | Product name | 4 | 20250516 |
| 30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2 | Product name | 5 | 20250304 |
| 334fe8d2-68fb-4331-a576-420e302ec069 | Product name | 7 | 20240320 |
| 444b3e50-f226-46ef-bfca-2e7035d140cd | Product name | 1 | 20190611 |
| e92765c1-be81-432a-b909-1b10777ec378 | Product name | 1 | 20190208 |
| 7cda52fc-125f-421c-8fea-bc1974370c49 | Product name | 2 | 20180703 |
| d5e51f11-ad28-caa4-4b49-4143974782ad | Product name | 1 | 20150831 |
| 0ca1d589-929b-4b33-bc5b-1d84abdafa6a | Product name | 1 | 20150324 |
| fc363c46-397b-4476-ac0f-70e43e8e4592 | Product name | 1 | 20150324 |
| 0441a8f5-3835-497c-aedd-bc78cba56b2a | Product name | 1 | 20150317 |
| 87711080-88eb-65c5-b2dd-bf99e700a372 | Product name | 1 | 20140508 |
| ec2149b3-5c6d-5344-f757-c86411073075 | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 0135-0243-02 | 2023-02-17 | C162847 | 48780-1 | e4f33bdf-ab64-d8a0-e053-dadaa90a6e4e | Drug Facts |
| 0135-0243-02 | 2022-07-29 | C162847 | 48780-1 | e4f33bdf-ab64-d8a0-e053-dadaa90a6e4e | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0135-0243-02 | TUMSSmoothies | 60 in 1 BOTTLE | TABLET, CHEWABLE | 60 | 21 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0135-0243-02 | EA - Each | 0135-0243 | 15306786-6eed-4d3f-840d-36940260027e | 1 | 2013-02-13 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| FEVIA Acid Control | CALCIUM CARBONATE | VIVUNT PHARMA LLC | 4d695a90-6502-3020-e063-6394a90ab0c3 | 2026-07-15 | Warnings | M001 |
| GOOD NEIGHBOR PHARMACY Antacid Extra Strength | ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE | Amerisource Bergen | 5e346dc0-69ce-4cc5-bb5d-bfa833e11c1f | 2026-07-13 | Warnings | M001 |
| Major Regular Strength Assorted Flavors | ANTACID TABLETS | Major Pharmaceuticals | 2ba0eeb2-7048-4259-83d5-9f4ec1c92d32 | 2026-07-13 | Warnings | M001 |
| Good Neighbor Extra Strength Assorted Fruits | CALCIUM CARBONATE | AMERISOURCE BERGEN | abf564a1-0823-433d-a023-8be4e085daf4 | 2026-07-13 | Warnings | M001 |
| Omeprazole, 24/7 Life by 7-Eleven | OMEPRAZOLE TABLET, DELAYED RELEASE | Lil' Drug Store Products, Inc. | 36d8a272-6cca-e759-e063-6394a90a9df8 | 2026-07-08 | Warnings | M001 |
| Tums Ultra | CALCIUM CARBONATE | Haleon US Holdings LLC | c544120f-15f0-48b5-88b2-d4820f180f50 | 2026-07-07 | Warnings | M001 |
| Regular Strength Assorted Flavors | ANTACID CALCIUM CARBONATE | AKRON PHARMA INC | 3f7fe022-aee9-b899-e063-6394a90afb4e | 2026-07-07 | Warnings | M001 |
| Magnesium Oxide | MAGNESIUM OXIDE | Westminster Pharmaceuticals, LLC | 52eeac0e-94bb-48c3-81dc-578e96406c01 | 2026-07-06 | Warnings | M001 |
| Kids Tummy Relief | CALCIUM CARBONATE | PNP Pharmaceuticals Inc. | 5103a317-5c4a-ec96-e063-6294a90aad7e | 2026-07-01 | Warnings | M001 |
| Childrens Antacid | CALCIUM CARBONATE | DOLGENCORP, LLC | 4d6ebc7e-ef39-47e8-91e9-f38484329fa9 | 2026-06-30 | Warnings | M001 |
| Ultra Strength Antacid | CALCIUM CARBONATE CHEWABLE TABLETS | CVS Pharmacy. Inc. | 24cec2bc-cf12-b513-e063-6394a90a9447 | 2026-06-30 | Warnings | M001 |
| Childrens Stomach Relief | CALCIUM CARBONATE | Chain Drug Marketing Association, Inc. | fb47d693-72d7-4586-9855-5e833ad1406f | 2026-06-18 | Warnings | M001 |
| Dr. Sana Alivio Digestivo UPSET STOMACH | EFEFERVESCENT ANTACID | EVI LABS | 51b8750c-3fcf-2543-e063-6394a90a7a8f | 2026-06-16 | Warnings | M001 |
| E-Z-GAS II | ANTACID/ANTIFLATULENT | E-Z-EM, INC. | 4e12e1cb-b033-076d-e054-00144ff8d46c | 2026-06-15 | Warnings | M001 |
| Sodium Bicarbonate | SODIUM BICARBONATE | Cardinal Health 107, LLC | 60c2a176-8854-4479-b853-d07fe9a1830c | 2026-06-12 | Warnings | M001 |
| Mag-Al Plus | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, AND SIMETHICONE | Cardinal Health 107, LLC | 08df7403-9ee3-4a43-a151-c1a6ef7a7549 | 2026-06-10 | Warnings | M001 |
| Childrens Antacid | CALCIUM CARBONATE | Rite Aid Corporation | d09c2d99-9a1f-4eae-a048-ab6dbf74a798 | 2026-06-09 | Warnings | M001 |
| Maximum Strength Calcium Carbonate 1000mg | CALCIUM CARBONATE CHEWABLE TABLETS | CVS HEALTH CORP | 24ce4597-b571-3cbf-e063-6394a90a8ea2 | 2026-06-09 | Warnings | M001 |
| Tums Chewy Bites with Gas Relief | CALCIUM CARBONATE AND SIMETHICONE | Haleon US Holdings LLC | 6d7be7e4-4bff-4cfd-bbbe-df412ac9db10 | 2026-06-09 | Warnings | M001 |
| Sodium Bicarbonate Antacid | SODIUM BICARBONATE | NCS HealthCare of KY, LLC dba Vangard Labs | fde4ea0c-152b-4b79-a6d8-2b0dbd9107aa | 2026-06-04 | Warnings | M001 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 308915 | calcium carbonate 750 MG (Ca 300 MG) Chewable Tablet | PSN | c22944b8-8733-4689-be0c-f320467f79ea | 21 |
| 1044532 | Tums Extra Strength 750 MG (Ca 300 MG) Chewable Tablet | PSN | c22944b8-8733-4689-be0c-f320467f79ea | 21 |
| 1044532 | calcium carbonate 750 MG Chewable Tablet [Tums] | SBD | c22944b8-8733-4689-be0c-f320467f79ea | 21 |
| 308915 | calcium carbonate 750 MG Chewable Tablet | SCD | c22944b8-8733-4689-be0c-f320467f79ea | 21 |
| 308915 | calcium carbonate 750 MG (calcium 300 MG) Chewable Tablet | SY | c22944b8-8733-4689-be0c-f320467f79ea | 21 |
| 1044532 | Tums Chewy Bites 750 MG Chewable Tablet | SY | c22944b8-8733-4689-be0c-f320467f79ea | 21 |
| 1044532 | Tums E-X 750 MG (calcium 300 MG) Chewable Tablet | SY | c22944b8-8733-4689-be0c-f320467f79ea | 21 |
| 1044532 | Tums Kids 750 MG Chewable Tablet | SY | c22944b8-8733-4689-be0c-f320467f79ea | 21 |
| 1044532 | Tums Smoothies 750 MG Chewable Tablet | SY | c22944b8-8733-4689-be0c-f320467f79ea | 21 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 0135-0243-02 | 00135024302 | 60 TABLET, CHEWABLE in 1 BOTTLE (0135-0243-02) | 2010-03-24 | 0000-00-00 | No | No | Current |