Home NDC 0135-0181 TUMS
Product NDC 0135-0181
11-digit product format 001350181
Labeler code 0135
Product ID 0135-0181_35c4dd66-0a1f-dda3-e063-6394a90a2c78
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 2026-12-31
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 · 8 matching rows.
View current auxiliary records. · View the auxiliary file history.
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
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# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0135-0181-01 TUMSULTRA 12 in 1 PACKAGE TABLET, CHEWABLE 12 19 0135-0181-01 TUMSULTRA 3 in 1 CARTON TABLET, CHEWABLE 3 19 0135-0181-02 TUMSULTRA 72 in 1 BOTTLE TABLET, CHEWABLE 72 19 0135-0181-03 TUMSULTRA 12 in 1 PACKAGE TABLET, CHEWABLE 12 19 0135-0181-05 TUMSULTRA 265 in 1 BOTTLE TABLET, CHEWABLE 265 19 0135-0181-06 TUMSULTRA 86 in 1 BOTTLE TABLET, CHEWABLE 86 19 0135-0181-07 TUMSULTRA 12 in 1 PACKAGE TABLET, CHEWABLE 12 19 0135-0181-07 TUMSULTRA 1 in 1 CARTON TABLET, CHEWABLE 1 19 0135-0181-14 TUMSULTRA 160 in 1 BOTTLE TABLET, CHEWABLE 160 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 0135-0181 TUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [HALEON US HOLDINGS LLC] 19 Current NDC, Legacy NDC, 9 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 1 of 37 · 739 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Dr. Sana Lemon Alivio Digestivo UPSET STOMACH EFFERVESCENT ANTACID EVI LABS 59cdf417-e5c0-6bb2-e063-6294a90a9c51 2026-08-24 Warnings Exact identifier application number: M001 Dr Sana Alivio Digestivo Naranja UPSET STOMACH EFFERVESCENT ANTACID EVI LABS 59d07c2d-ef11-bd32-e063-6394a90af87d 2026-08-24 Warnings Exact identifier application number: M001 Genexa Antacid Maximum Strength CALCIUM CARBONATE Genexa Inc. 3a39d91c-2dcd-71d6-e063-6394a90a5474 2026-08-22 Warnings Exact identifier application number: M001 Mag-AL Plus ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, AND SIMETHICONE PAI Holdings, LLC dba PAI Pharma 896ab07a-1b40-43ab-8589-3be86b1c4198 2026-08-19 Warnings Exact identifier application number: M001 CVS Health Extra Strength Antacid ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE CVS PHARMACY 8629529e-4363-4d37-9ae0-27193868df32 2026-08-19 Warnings Exact identifier application number: M001 CVS Naturals CALCIUM CARBONATE CVS PHARMACY 899f057a-914d-49ca-a9fd-9fc48149782a 2026-08-14 Warnings Exact identifier application number: M001 CVS Health Extra Strength Heartburn Relief Antacid Original Flavor ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE CVS Pharmacy,Inc. 5c32d90b-68a0-4acf-94b6-d02037cea376 2026-08-13 Warnings Exact identifier application number: M001 Extra Strength Smooth ANTACID TABLETS CVS c00204f7-c343-4451-9e0f-638ebb72f07c 2026-08-13 Warnings Exact identifier application number: M001 CVS PHARMACY Extra Strength Cherry Flavor ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE CVS Pharmacy,Inc. cf7ae053-fa8d-4e6e-af4f-b846699aaf24 2026-08-13 Warnings Exact identifier application number: M001 CVS Extra Strength Smooth CALCIUM CARBONATE CVS PHARMACY 70752251-02fe-4639-a4a8-afef32463c32 2026-08-13 Warnings Exact identifier application number: M001 CVS PHARMACY,INC. Assorted Berry ANTACID TABLETS CVS PHARMACY,INC. 19f0847e-1512-465c-b67f-d61ef4a16cfa 2026-08-12 Warnings Exact identifier application number: M001 CVS PHARMACY Assorted Berry Antacid CALCIUM CARBONATE CVS 7f0a4d88-4e3c-448e-90b1-ae03966b7806 2026-08-12 Warnings Exact identifier application number: M001 Extra Strength ANTACID TABLETS CVS PHARMACY f3cd6627-cd82-4d39-9593-55f016c72eec 2026-08-12 Warnings Exact identifier application number: M001 CVS Health Extra Strength Sugar Free ANTACID CVS PHARMACY, INC. 49e23561-d392-415c-9e6f-2dbcf64c9636 2026-08-12 Warnings Exact identifier application number: M001 CVS PHARMACY Assorted Fruit Antacid CALCIUM CARBONATE CVS 8ab371eb-9839-47f0-b576-d917f69ed16d 2026-08-12 Warnings Exact identifier application number: M001 CVS Ultra Strength ANTACID TABLETS CVS 6108271a-4336-4f90-9765-9c3aea109488 2026-08-12 Warnings Exact identifier application number: M001 CVS PHARMACY,INC. Assorted Fruit ANTACID TABLETS CVS PHARMACY,INC. 60294e90-4b9c-4419-876c-3da037d76cfd 2026-08-12 Warnings Exact identifier application number: M001 Whole Foods Market Regular Strength Peppermint Flavor CALCIUM CARBONATE WHOLE FOODS MARKET, INC. 4cdf0cd0-f69f-4f86-a9ff-cda5cb002d65 2026-08-11 Warnings Exact identifier application number: M001 Whole Foods Market Regular Strength Peppermint Flavor CALCIUM CARBONATE WHOLE FOODS MARKET, INC. ec3f0e47-52f3-4ffd-a3d3-71ef4bd11f08 2026-08-11 Warnings Exact identifier application number: M001 Whole Foods Market Regular Strength Peppermint Flavor CALCIUM CARBONATE WHOLE FOODS MARKET, INC. 639665ca-476e-4fbf-9378-a08cb28c15f6 2026-08-11 Warnings Exact identifier application number: M001
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 0135-0181-01 00135018101 3 PACKAGE in 1 CARTON (0135-0181-01) / 12 TABLET, CHEWABLE in 1 PACKAGE 3 package 2010-02-12 0000-00-00 No No Current 0135-0181-02 00135018102 72 TABLET, CHEWABLE in 1 BOTTLE (0135-0181-02) 2010-02-12 0000-00-00 No No Current 0135-0181-03 00135018103 12 TABLET, CHEWABLE in 1 PACKAGE (0135-0181-03) 2010-02-12 0000-00-00 No No Current 0135-0181-05 00135018105 265 TABLET, CHEWABLE in 1 BOTTLE (0135-0181-05) 2010-02-12 0000-00-00 No No Current 0135-0181-06 00135018106 86 TABLET, CHEWABLE in 1 BOTTLE (0135-0181-06) 2010-02-12 0000-00-00 No No Current 0135-0181-07 00135018107 1 PACKAGE in 1 CARTON (0135-0181-07) / 12 TABLET, CHEWABLE in 1 PACKAGE 1 package 2010-02-12 0000-00-00 No No Current 0135-0181-14 00135018114 160 TABLET, CHEWABLE in 1 BOTTLE (0135-0181-14) 2010-02-12 0000-00-00 No No Current