Home NDC 0135-0243 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.
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 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 table Ingredient Strength CALCIUM CARBONATE 750 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination H0G9379FGK Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 308915 Internal RxNorm lookup 1044532 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 0135-0243-02 TUMSSmoothies 60 in 1 BOTTLE TABLET, CHEWABLE 60 21
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded CALCIUM CARBONATE ACTIVE INGREDIENT H0G9379FGK TUMS SMOOTHIES (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 10 CARBONATE ION ACTIVE MOIETY 7UJQ5OPE7D TUMS SMOOTHIES (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 10 ADIPIC ACID INACTIVE INGREDIENT 76A0JE0FKJ TUMS SMOOTHIES (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 10 ALUMINUM OXIDE INACTIVE INGREDIENT LMI26O6933 TUMS SMOOTHIES (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 10 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U TUMS SMOOTHIES (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 10 DEXTROSE INACTIVE INGREDIENT IY9XDZ35W2 TUMS SMOOTHIES (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 10 FD&C BLUE NO. 1 INACTIVE INGREDIENT H3R47K3TBD TUMS SMOOTHIES (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 10 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA TUMS SMOOTHIES (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 10 FD&C YELLOW NO. 5 INACTIVE INGREDIENT I753WB2F1M TUMS SMOOTHIES (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 10 FD&C YELLOW NO. 6 INACTIVE INGREDIENT H77VEI93A8 TUMS SMOOTHIES (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 10 GUAR GUM INACTIVE INGREDIENT E89I1637KE TUMS SMOOTHIES (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 10 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 TUMS SMOOTHIES (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 10 MALTODEXTRIN INACTIVE INGREDIENT 7CVR7L4A2D TUMS SMOOTHIES (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 10 SORBITOL INACTIVE INGREDIENT 506T60A25R TUMS SMOOTHIES (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 10 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ TUMS SMOOTHIES (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 10 SUCROSE INACTIVE INGREDIENT C151H8M554 TUMS SMOOTHIES (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP] 10
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0135-0243 TUMS SMOOTHIES (CALCIUM CARBONATE) TABLET, CHEWABLE [HALEON US HOLDINGS LLC] 20 Current NDC, Legacy NDC, 1 package rows 20250228_c22944b8-8733-4689-be0c-f320467f79ea.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 10 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 0135-0243-02 00135024302 60 TABLET, CHEWABLE in 1 BOTTLE (0135-0243-02) 2010-03-24 0000-00-00 No No Current