FDA.reportPublic FDA data

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

Additional Listing Data#

Finished product
Yes
Brand name base
TUMS
Brand name suffix
ULTRA
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CALCIUM CARBONATE1000 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiH0G9379FGK
Rxcui308892, 1044524

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
e92765c1-be81-432a-b909-1b10777ec378Product name120190208
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0135-0181-012020-12-01C16284748780-19d75b9d0-c409-f424-e053-dadaa90a57ceDrug Facts
0135-0181-022020-12-01C16284748780-19d75b9d0-c409-f424-e053-dadaa90a57ceDrug Facts
0135-0181-032020-12-01C16284748780-19d75b9d0-c409-f424-e053-dadaa90a57ceDrug Facts
0135-0181-052020-12-01C16284748780-19d75b9d0-c409-f424-e053-dadaa90a57ceDrug Facts
0135-0181-062020-12-01C16284748780-19d75b9d0-c409-f424-e053-dadaa90a57ceDrug Facts
0135-0181-072020-12-01C16284748780-19d75b9d0-c409-f424-e053-dadaa90a57ceDrug Facts
0135-0181-142020-12-01C16284748780-19d75b9d0-c409-f424-e053-dadaa90a57ceDrug Facts
0135-0181-012020-01-31C16284748780-19d75b9d0-c409-f424-e053-dadaa90a57ceDrug Facts
0135-0181-022020-01-31C16284748780-19d75b9d0-c409-f424-e053-dadaa90a57ceDrug Facts
0135-0181-032020-01-31C16284748780-19d75b9d0-c409-f424-e053-dadaa90a57ceDrug Facts
0135-0181-052020-01-31C16284748780-19d75b9d0-c409-f424-e053-dadaa90a57ceDrug Facts
0135-0181-062020-01-31C16284748780-19d75b9d0-c409-f424-e053-dadaa90a57ceDrug Facts
0135-0181-072020-01-31C16284748780-19d75b9d0-c409-f424-e053-dadaa90a57ceDrug Facts
0135-0181-142020-01-31C16284748780-19d75b9d0-c409-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0135-0181-01TUMSULTRA12 in 1 PACKAGETABLET, CHEWABLE1219
0135-0181-01TUMSULTRA3 in 1 CARTONTABLET, CHEWABLE319
0135-0181-02TUMSULTRA72 in 1 BOTTLETABLET, CHEWABLE7219
0135-0181-03TUMSULTRA12 in 1 PACKAGETABLET, CHEWABLE1219
0135-0181-05TUMSULTRA265 in 1 BOTTLETABLET, CHEWABLE26519
0135-0181-06TUMSULTRA86 in 1 BOTTLETABLET, CHEWABLE8619
0135-0181-07TUMSULTRA12 in 1 PACKAGETABLET, CHEWABLE1219
0135-0181-07TUMSULTRA1 in 1 CARTONTABLET, CHEWABLE119
0135-0181-14TUMSULTRA160 in 1 BOTTLETABLET, CHEWABLE16019

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0135-0181-01EA - Each0135-01813ca8e9eb-8f24-49a3-aa76-d454a879203612013-02-13
0135-0181-02EA - Each0135-01816118ebcd-49f3-4bc0-9d3c-97038cfba83b12013-07-02
0135-0181-03EA - Each0135-01811ab8b6e7-f1d8-4a9a-b3a1-dcfabacecf5d12012-07-24
0135-0181-05EA - Each0135-01815a64400c-be72-4160-b361-3cb94d44934912012-07-24
0135-0181-07EA - Each0135-0181b64d8086-5e12-4121-957f-0eb3a2f33a3312025-05-14
0135-0181-14EA - Each0135-018153c3be7d-8bc7-43e1-9b06-d3f7f5d491eb12012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CALCIUM CARBONATEACTIVE INGREDIENTH0G9379FGKTUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP]9
CALCIUM CATIONACTIVE MOIETY2M83C4R6ZBTUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP]9
ADIPIC ACIDINACTIVE INGREDIENT76A0JE0FKJTUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP]9
ALUMINUM OXIDEINACTIVE INGREDIENTLMI26O6933TUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP]9
FD&C BLUE NO. 1INACTIVE INGREDIENTH3R47K3TBDTUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP]9
FD&C RED NO. 40INACTIVE INGREDIENTWZB9127XOATUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP]9
FD&C YELLOW NO. 5INACTIVE INGREDIENTI753WB2F1MTUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP]9
FD&C YELLOW NO. 6INACTIVE INGREDIENTH77VEI93A8TUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP]9
MINERAL OILINACTIVE INGREDIENTT5L8T28FGPTUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP]9
SODIUM POLYMETAPHOSPHATEINACTIVE INGREDIENTP1BM4ZH95LTUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP]9
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJTUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP]9
SUCROSEINACTIVE INGREDIENTC151H8M554TUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP]9
TALCINACTIVE INGREDIENT7SEV7J4R1UTUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEATHCARE LP]9

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0135-0181TUMS ULTRA (CALCIUM CARBONATE) TABLET, CHEWABLE [HALEON US HOLDINGS LLC]19Current NDC, Legacy NDC, 9 package rows20250524_f4786707-a0f7-4ba8-9656-06278d1b4b6c.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
308892calcium carbonate 1000 MG (Ca 400 MG) Chewable TabletPSNf4786707-a0f7-4ba8-9656-06278d1b4b6c19
1044524Tums Ultra 1000 MG (Ca 400 MG) Chewable TabletPSNf4786707-a0f7-4ba8-9656-06278d1b4b6c19
1044524calcium carbonate 1000 MG Chewable Tablet [Tums]SBDf4786707-a0f7-4ba8-9656-06278d1b4b6c19
308892calcium carbonate 1000 MG Chewable TabletSCDf4786707-a0f7-4ba8-9656-06278d1b4b6c19
308892calcium carbonate 1000 MG (calcium 400 MG) Chewable TabletSYf4786707-a0f7-4ba8-9656-06278d1b4b6c19
1044524Tums 1000 MG Chewable TabletSYf4786707-a0f7-4ba8-9656-06278d1b4b6c19
1044524Tums Ultra 1000 MG (calcium 400 MG) Chewable TabletSYf4786707-a0f7-4ba8-9656-06278d1b4b6c19

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0135-0181-01001350181013 PACKAGE in 1 CARTON (0135-0181-01) / 12 TABLET, CHEWABLE in 1 PACKAGE3 package2010-02-120000-00-00NoNoCurrent
0135-0181-020013501810272 TABLET, CHEWABLE in 1 BOTTLE (0135-0181-02) 2010-02-120000-00-00NoNoCurrent
0135-0181-030013501810312 TABLET, CHEWABLE in 1 PACKAGE (0135-0181-03) 2010-02-120000-00-00NoNoCurrent
0135-0181-0500135018105265 TABLET, CHEWABLE in 1 BOTTLE (0135-0181-05) 2010-02-120000-00-00NoNoCurrent
0135-0181-060013501810686 TABLET, CHEWABLE in 1 BOTTLE (0135-0181-06) 2010-02-120000-00-00NoNoCurrent
0135-0181-07001350181071 PACKAGE in 1 CARTON (0135-0181-07) / 12 TABLET, CHEWABLE in 1 PACKAGE1 package2010-02-120000-00-00NoNoCurrent
0135-0181-1400135018114160 TABLET, CHEWABLE in 1 BOTTLE (0135-0181-14) 2010-02-120000-00-00NoNoCurrent