Home NDC 0135-0641 Tums Chewy Bites
Product NDC 0135-0641
11-digit product format 001350641
Labeler code 0135
Product ID 0135-0641_12b447a1-1d24-383f-e063-6394a90affdd
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 2021-01-15
Substance CALCIUM CARBONATE
Active strength 1000 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 Chewy Bites
Brand name suffix Mixed Fruit
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM CARBONATE 1000 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 308892 Internal RxNorm lookup 1044524 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0135-0641-03 Tums Chewy BitesMixed Fruit 54 in 1 BOTTLE TABLET, CHEWABLE 54 4 0135-0641-03 Tums Chewy BitesMixed Fruit 3 in 1 PACKAGE TABLET, CHEWABLE 3 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0135-0641 TUMS CHEWY BITES MIXED FRUIT (CALCIUM CARBONATE) TABLET, CHEWABLE [HALEON US HOLDINGS LLC] 4 Current NDC, Legacy NDC, 2 package rows 20240304_d341b832-edcf-4cb2-96e1-c303b030c59a.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 0135-0641-03 00135064103 3 BOTTLE in 1 PACKAGE (0135-0641-03) / 54 TABLET, CHEWABLE in 1 BOTTLE 3 bottle 2021-01-15 0000-00-00 No No Current