Home NDC 0135-0076 TUMS
Product NDC 0135-0076
11-digit product format 001350076
Labeler code 0135
Product ID 0135-0076_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 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 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 0135-0076-01 TUMSEX 116 in 1 BOTTLE TABLET 116 18 0135-0076-25 TUMSEX 96 in 1 BOTTLE TABLET 96 18 0135-0076-26 TUMSEX 70 in 1 BOTTLE TABLET 70 18
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0135-0076 TUMS EX (CALCIUM CARBONATE) TABLET [HALEON US HOLDINGS LLC] 18 Current NDC, Legacy NDC, 3 package rows 20241207_593a0494-d669-4bcf-8412-b92645b2d76c.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 Units Marketing start Marketing end Sample Exclude flag Status 0135-0076-01 00135007601 116 TABLET in 1 BOTTLE (0135-0076-01) 116 tablet 2010-01-18 0000-00-00 No No Current 0135-0076-25 00135007625 96 TABLET in 1 BOTTLE (0135-0076-25) 96 tablet 2010-01-18 0000-00-00 No No Current 0135-0076-26 00135007626 70 TABLET in 1 BOTTLE (0135-0076-26) 70 tablet 2010-01-18 0000-00-00 No No Current