Home NDC 0135-0540 TUMS
Product NDC 0135-0540
11-digit product format 001350540
Labeler code 0135
Product ID 0135-0540_5ca009f2-85d1-1387-e063-6294a90ac707
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 2010-02-12
Substance CALCIUM CARBONATE
Active strength 1000 mg/1
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.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2020-06-10 20:45 UTC · source 2020-06-10 excluded product product 0135-0540 I Inactivated by FDA excluded / ndc_excluded.zip 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 0135-0540 0135-0540-01 I Inactivated by FDA excluded / ndc_excluded.zip 9bebd1f3094a…5416666fcb17…
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 ULTRA
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM CARBONATE 1000 mg/1
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0135-0540-01 TUMSULTRA 86 in 1 BOTTLE TABLET, CHEWABLE 86 19
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded CALCIUM CARBONATE ACTIVE INGREDIENT H0G9379FGK TUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 9 CALCIUM CATION ACTIVE MOIETY 2M83C4R6ZB TUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 9 ADIPIC ACID INACTIVE INGREDIENT 76A0JE0FKJ TUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 9 ALUMINUM OXIDE INACTIVE INGREDIENT LMI26O6933 TUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 9 FD&C BLUE NO. 1 INACTIVE INGREDIENT H3R47K3TBD TUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 9 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA TUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 9 FD&C YELLOW NO. 5 INACTIVE INGREDIENT I753WB2F1M TUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 9 FD&C YELLOW NO. 6 INACTIVE INGREDIENT H77VEI93A8 TUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 9 MINERAL OIL INACTIVE INGREDIENT T5L8T28FGP TUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 9 SODIUM POLYMETAPHOSPHATE INACTIVE INGREDIENT P1BM4ZH95L TUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 9 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ TUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 9 SUCROSE INACTIVE INGREDIENT C151H8M554 TUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 9 TALC INACTIVE INGREDIENT 7SEV7J4R1U TUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0135-0540 TUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [HALEON US HOLDINGS LLC] 19 Current NDC, Legacy NDC, 1 package rows 20250524_f4786707-a0f7-4ba8-9656-06278d1b4b6c.zip
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.
Matched openFDA labels page 18 of 34 · 678 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Extra Strength Smooth Antacid ANTACID TABLETS Wal-Mart Stores,Inc., 92372491-000d-4273-a668-b87722c1d381 2025-10-27 Warnings Exact identifier application number: M001 equate Extra Strength Smooth Antacid Assorted Berries ANTACID TABLETS Wal-Mart Stores,Inc., cc93e3b4-adbc-4a2c-b6fc-bf7456ef1656 2025-10-27 Warnings Exact identifier application number: M001 Magnesium Oxide MAGNESIUM OXIDE Kesin Pharma 31f417f0-1637-eefa-e063-6294a90a121b 2025-10-27 Warnings Exact identifier application number: M001 Rugby Extra Strength Assorted Berries ANTACID TABLETS Rugby Laboratories b0fcfd66-276e-4741-9aee-915b6364f25c 2025-10-25 Warnings Exact identifier application number: M001 Rugby ANTACID TABLETS Rugby Laboratories 9cb56bc3-7075-4f81-bd10-7e602034b7d8 2025-10-25 Warnings Exact identifier application number: M001 Rugby Cal-Gest Antacid Assorted Flavors ANTACID TABLETS Rugby Laboratories, Inc. a43184c4-d225-4539-b651-4d96535f208f 2025-10-25 Warnings Exact identifier application number: M001 Super vitamin C serum SUPER VITAMIN C FlexiGo Inc 41cbe84e-3ddf-b806-e063-6294a90a55a4 2025-10-22 Warnings Exact identifier application number: M001 Exchange Select Antacid Soft Chews Cherry Flavor CALCIUM CARBONATE Army & Air Force Exchange Service 41ad5581-5b8a-1c8b-e063-6294a90a2ba6 2025-10-21 Warnings Exact identifier application number: M001 Magnesium Oxide MAGNESIUM OXIDE Method Pharmaceuticals, LLC 0af63651-f9d9-43b9-b6f0-4878466a82e6 2025-10-21 Warnings Exact identifier application number: M001 CardinalExtra Strength Antacid Wintergreen flavor CALCIUM CARBONATE CARDINAL HEALTH 4e40989f-c710-442a-bb8d-02e813ddf04d 2025-10-14 Warnings Exact identifier application number: M001 Regular Strength Antacid Assorted Fruit CALCIUM CARBONATE CARDINAL HEALTH def9eaef-308f-49f2-898b-469c2c395d27 2025-10-14 Warnings Exact identifier application number: M001 Leader Extra Strength Sugar Free Antacid ANTACID Cardinal Health d7a6f1b8-bdf7-45bb-bab0-b22f45e78440 2025-10-14 Warnings Exact identifier application number: M001 Extra Strength Antacid Original Flavor ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE Cardinal Health 1fe459f6-be7f-4c59-b33b-f13ec17071f2 2025-10-14 Warnings Exact identifier application number: M001 Cardinal Extra Strength Smooth Antacid Assorted Fruits CALCIUM CARBONATE CARDINAL HEALTH 84bf7fea-a071-4583-9453-1aea4d198ca6 2025-10-14 Warnings Exact identifier application number: M001 ANTACID Extra Strength CALCIUM CARBONATE Cardinal Health 110, LLC. 3ce9b97b-1680-4299-9a2c-132318adbc0c 2025-10-14 Warnings Exact identifier application number: M001 ANTACID Extra Strength CALCIUM CARBONATE CARDINAL HEALTH 110, LLC. 7c1b2ee6-b691-4c12-bed5-f0a360ad46bb 2025-10-14 Warnings Exact identifier application number: M001 ANTACID Ultra Strength CALCIUM CARBONATE CARDINAL HEALTH 110, LLC. d267ca31-09bd-46d3-be08-a259642f1b7f 2025-10-14 Warnings Exact identifier application number: M001 Magnesium Oxide MAGNESIUM OXIDE A-S Medication Solutions c14d2b4d-d6d8-4293-835e-5d893d5b7e6a 2025-10-10 Warnings Exact identifier application number: M001 Calcium Carbonate Antacid Assorted Berries CALCIUM CARBONATE Xiamen Kang Zhongyuan Biotechnology Co., Ltd. 3f640ccd-4b8d-fc24-e063-6294a90a6e58 2025-09-22 Warnings Exact identifier application number: M001 Stomachin Antacid MAGNESIUM CARBONATE AND SODIUM BICARBONATE Chang Kuo Chou Pharmaceutical Co., Ltd. 60fa0650-8785-4cb3-8f88-1a437296252f 2025-09-19 Warnings Exact identifier application number: M001
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 0135-0540-01 00135054001 86 TABLET, CHEWABLE in 1 BOTTLE (0135-0540-01) 2010-02-12 0000-00-00 No No Current