Home NDC 0135-0228 TUMS
Product NDC 0135-0228
11-digit product format 001350228
Labeler code 0135
Product ID 0135-0228_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 · 17 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 0135-0228-07 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 0135-0228-07 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 0135-0228-07 D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 0135-0228-07 D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 0135-0228-07 D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 0135-0228-07 D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 0135-0228-07 D Discontinued by firm 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 0135-0228-07 D Discontinued by firm ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 0135-0228-07 D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 0135-0228-07 D Discontinued by firm ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 0135-0228-07 D Discontinued by firm 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 0135-0228-07 D Discontinued by firm 557ba5c1ecfa…9c80585c8c6e…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 0135-0228-01 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 0135-0228-05 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 0135-0228-06 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 0135-0228-04 I Inactivated by FDA 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 0135-0228-01 TUMSULTRA 12 in 1 PACKAGE TABLET, CHEWABLE 12 19 0135-0228-04 TUMSULTRA 10 in 1 PACKAGE TABLET, CHEWABLE 10 19 0135-0228-05 TUMSULTRA 160 in 1 BOTTLE TABLET, CHEWABLE 160 19 0135-0228-06 TUMSULTRA 72 in 1 BOTTLE TABLET, CHEWABLE 72 19 0135-0228-07 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 0135-0228 TUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [HALEON US HOLDINGS LLC] 19 Current NDC, Legacy NDC, 5 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 8 of 34 · 678 matching rows.
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 0135-0228-01 00135022801 12 TABLET, CHEWABLE in 1 PACKAGE (0135-0228-01) 2010-02-12 0000-00-00 No No Current 0135-0228-04 00135022804 10 TABLET, CHEWABLE in 1 PACKAGE (0135-0228-04) 2010-02-12 0000-00-00 No No Current 0135-0228-05 00135022805 160 TABLET, CHEWABLE in 1 BOTTLE (0135-0228-05) 2010-02-12 0000-00-00 No No Current 0135-0228-06 00135022806 72 TABLET, CHEWABLE in 1 BOTTLE (0135-0228-06) 2010-02-12 0000-00-00 No No Current 0135-0228-07 00135022807 86 in 1 BOTTLE Historical