TUMS
- Product NDC
- 0135-0178
- 11-digit product format
- 001350178
- Labeler code
- 0135
- Product ID
- 0135-0178_3ce3175f-47e7-4ea3-b5b6-836368fc7522
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- calcium carbonate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Haleon US Holdings LLC
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2010-01-18
- 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
- 2026-12-31
- Current FDA listing
- Yes
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 0135-0178 | 0135-0178-01 | D | Discontinued by firm | 2026-10-15 |
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 | Snapshot | Source SHA-256 |
|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | cdf11ea48f46… | ba0047e9e063… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | 0efc9e666f02… | f202fb6c5f17… |
| 2024-11-09 02:27 UTC · source 2024-11-08 | ad56d346431e… | cc804d4bbf1e… |
| 2024-10-04 04:10 UTC · source 2024-10-03 | 367a005e9d99… | 383a685ebd0f… |
| 2024-07-10 04:00 UTC · source 2024-07-09 | 557ba5c1ecfa… | 9c80585c8c6e… |
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
- EX
- Listing expiration
- 2026-12-31
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 |
|---|---|
| 593a0494-d669-4bcf-8412-b92645b2d76c | 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 | Related label |
|---|---|---|
| 0135-0178-01 | 2020-02-28 | Drug Facts |
| 0135-0178-02 | 2020-02-28 | Drug Facts |
| 0135-0178-03 | 2020-02-28 | Drug Facts |
| 0135-0178-05 | 2020-02-28 | Drug Facts |
| 0135-0178-08 | 2020-02-28 | Drug Facts |
| 0135-0178-09 | 2020-02-28 | Drug Facts |
| 0135-0178-01 | 2020-01-31 | Drug Facts |
| 0135-0178-02 | 2020-01-31 | Drug Facts |
| 0135-0178-03 | 2020-01-31 | Drug Facts |
| 0135-0178-05 | 2020-01-31 | Drug Facts |
| 0135-0178-08 | 2020-01-31 | Drug Facts |
| 0135-0178-09 | 2020-01-31 | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0135-0178-01 | TUMSEX | 116 in 1 BOTTLE | TABLET | 116 | 18 | |
| 0135-0178-02 | TUMSEX | 48 in 1 BOTTLE | TABLET | 48 | 18 | |
| 0135-0178-03 | TUMSEX | 96 in 1 BOTTLE | TABLET | 96 | 18 | |
| 0135-0178-05 | TUMSEX | 70 in 1 BOTTLE | TABLET | 70 | 18 | |
| 0135-0178-08 | TUMSEX | 8 in 1 PACKAGE | TABLET | 8 | 18 | |
| 0135-0178-09 | TUMSEX | 200 in 1 BOTTLE | TABLET | 200 | 18 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0135-0178-02 | EA - Each | 0135-0178 | aa0dead0-393e-4f86-a678-29842845c6b1 | 1 | 2012-07-24 |
| 0135-0178-03 | EA - Each | 0135-0178 | 828a68d4-668d-42ed-bba1-f340b3d73b4e | 1 | 2012-07-24 |
| 0135-0178-08 | EA - Each | 0135-0178 | 1c31cdb9-111a-460f-add0-c55b1f997c45 | 1 | 2012-07-24 |
| 0135-0178-09 | EA - Each | 0135-0178 | 4338679f-0c13-4bd5-9293-15b0e28be12d | 1 | 2017-04-05 |
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 |
|---|---|---|---|---|---|---|
| SUPREME ANTACID | CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | FAMILY DOLLAR SERVICES INC | 5e996df3-25a4-b259-e053-2a91aa0a4311 | 2025-11-19 | Warnings | M001 |
| GERI-LANTA ANTACID ANTIGAS | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE | Geri-Care Pharmaceuticals, Corp | a7d7298f-44d6-4e09-8578-7fe311243002 | 2025-11-19 | Warnings | M001 |
| GERI-MOX MAX CHERRY | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE | Geri-Care Pharmaceuticals, Corp | 8e57bcf5-2960-4c41-8bf2-83cb1ee50168 | 2025-11-19 | Warnings | M001 |
| Tums Antacid Chewy Bites | CALCIUM CARBONATE 750 MG | R J General Corporation | 6208d11d-0670-4a20-a3fc-ebc764a8e6cd | 2025-11-17 | Warnings | M001 |
| REGULAR STRENGTH ANTACID/ANTIGAS | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE | RUGBY LABORATORIES | b244fce9-9626-e947-e053-2995a90ab8f9 | 2025-11-17 | Warnings | M001 |
| Antacid Childrens | CALCIUM CARBONATE | CVS Pharmacy | 08953df1-cc29-452f-bc69-b19970a1fd2e | 2025-11-15 | Warnings | M001 |
| Magnesium Oxide | MAGNESIUM OXIDE | Marlex Pharmaceuticals Inc | 0bb322a5-fb92-14de-e063-6294a90a4c1b | 2025-11-14 | Warnings | M001 |
| magnesium oxide | MAGNESIUM OXIDE | Marlex Pharmaceuticals Inc. | dc57893c-068a-37d8-e053-2a95a90aa054 | 2025-11-14 | Warnings | M001 |
| Earthmed Soothe Chewable Orange | CITRIC ACID | Earthmed LLC | 439543fe-ceb9-4c5c-e063-6294a90a9b70 | 2025-11-14 | Warnings | M001 |
| MAXIMUM STRENGTH ANTACID MINT | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE | CVS | 3ce054f3-2953-5f7d-e054-00144ff8d46c | 2025-11-11 | Warnings | M001 |
| Topcare Antacid Extra Strength Assorted Berry | CALCIUM CARBONATE | Topco Associates LLC | 14f6f475-32d6-4783-8dcc-1fe265902d55 | 2025-11-10 | Warnings | M001 |
| Topcare Antacid Calcium | CALCIUM CARBONATE | Topco Associates LLC | 38c26f49-fb5e-480c-9164-bf5edcf0726b | 2025-11-10 | Warnings | M001 |
| Topcare Antacid Calcium | CALCIUM CARBONATE | Topco Associates LLC. | bb99b942-1f84-43e1-a18d-3a975cddc59e | 2025-11-08 | Warnings | M001 |
| Topcare Antacid Calcium Regular Strength | CALCIUM CARBONATE | Topco Associates LLC | 2606ac08-9760-4ff6-8d90-51fbb04e6ac8 | 2025-11-08 | Warnings | M001 |
| Topcare Antacid Calcium Extra Strength | CALCIUM CARBONATE | Topco Associates LLC | 495d97b0-d95c-46d1-a76a-56ac7f823538 | 2025-11-08 | Warnings | M001 |
| Topcare Antacid Calcium Extra Strength | CALCIUM CARBONATE | Topco Associates LLC. | 73b4cda2-900a-4380-a0ae-0abfecdb7263 | 2025-11-08 | Warnings | M001 |
| Topcare Extra Strength Antacid Assorted Fruit | CALCIUM CARBONATE | Topco Associates LLC | 2677ca2b-b211-475e-a9c4-643fd54a744f | 2025-11-08 | Warnings | M001 |
| TopCare Antacid Calcium | CALCIUM CARBONATE | Topco Associates LLC | b94eac38-62d0-49a2-bb49-053fda8129e2 | 2025-11-08 | Warnings | M001 |
| Topcare Antacid Calcium | CALCIUM CARBONATE | Topco Associates LLC | 04b3d397-df99-44e2-a191-6e9199b08398 | 2025-11-08 | Warnings | M001 |
| topcare Antacid Calcium Ultra Strength | CALCIUM CARBONATE | Topco Associates LLC | 6e2788b3-1e33-4908-aa2c-475d69b94ee6 | 2025-11-08 | Warnings | M001 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 308915 | calcium carbonate 750 MG (Ca 300 MG) Chewable Tablet | PSN | 593a0494-d669-4bcf-8412-b92645b2d76c | 18 |
| 1044532 | Tums Extra Strength 750 MG (Ca 300 MG) Chewable Tablet | PSN | 593a0494-d669-4bcf-8412-b92645b2d76c | 18 |
| 1044532 | calcium carbonate 750 MG Chewable Tablet [Tums] | SBD | 593a0494-d669-4bcf-8412-b92645b2d76c | 18 |
| 308915 | calcium carbonate 750 MG Chewable Tablet | SCD | 593a0494-d669-4bcf-8412-b92645b2d76c | 18 |
| 308915 | calcium carbonate 750 MG (calcium 300 MG) Chewable Tablet | SY | 593a0494-d669-4bcf-8412-b92645b2d76c | 18 |
| 1044532 | Tums Chewy Bites 750 MG Chewable Tablet | SY | 593a0494-d669-4bcf-8412-b92645b2d76c | 18 |
| 1044532 | Tums E-X 750 MG (calcium 300 MG) Chewable Tablet | SY | 593a0494-d669-4bcf-8412-b92645b2d76c | 18 |
| 1044532 | Tums Kids 750 MG Chewable Tablet | SY | 593a0494-d669-4bcf-8412-b92645b2d76c | 18 |
| 1044532 | Tums Smoothies 750 MG Chewable Tablet | SY | 593a0494-d669-4bcf-8412-b92645b2d76c | 18 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0135-0178-01 | 00135017801 | 116 in 1 BOTTLE | Historical | |||||
| 0135-0178-02 | 00135017802 | 48 TABLET in 1 BOTTLE (0135-0178-02) | 48 tablet | 2010-01-18 | 0000-00-00 | No | No | Current |
| 0135-0178-03 | 00135017803 | 96 TABLET in 1 BOTTLE (0135-0178-03) | 96 tablet | 2010-01-18 | 0000-00-00 | No | No | Current |
| 0135-0178-05 | 00135017805 | 70 TABLET in 1 BOTTLE (0135-0178-05) | 70 tablet | 2010-01-18 | 0000-00-00 | No | No | Current |
| 0135-0178-08 | 00135017808 | 8 TABLET in 1 PACKAGE (0135-0178-08) | 8 tablet | 2010-01-18 | 0000-00-00 | No | No | Current |
| 0135-0178-09 | 00135017809 | 200 TABLET in 1 BOTTLE (0135-0178-09) | 200 tablet | 2010-01-18 | 0000-00-00 | No | No | Current |