FDA.reportPublic FDA data

up and up extra strength smooth dissolving antacid

Manufacturer
Target corporation
Effective date
2015-01-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:45:15

Label at a glance#

Productup and up extra strength smooth dissolving antacid Assorted Fruit
Active ingredientCALCIUM CARBONATE
Label structure8 sections

Indications and uses

relieves • heartburn • acid indigestion • sour stomach • upset stomach associated with these symptoms

Dosage and administration

  adults and children 12 years of age and over: chew 2-4 tablets as symptoms occur, or as directed by a doctor   do not take for symptoms that persist for more than 2 weeks unless advised by a doctor

Label contents#

Full prescribing information#

Active ingredient (per tablet)

OTC - ACTIVE INGREDIENT SECTION

Calcium Carbonate USP 750mg

Purpose

OTC - PURPOSE SECTION

Antacid

Uses

INDICATIONS & USAGE SECTION

relieves

  • heartburn
  • acid indigestion
  • sour stomach
  • upset stomach associated with these symptoms

Warnings

WARNINGS SECTION

Ask a doctor or pharmacist before use if you are presentlytaking a prescription drug. Antacids may interact with certain prescription drugs.

When using this product

  • do not take more than 10 tablets in 24 hours
  • if pregnant do not take more than 6 tablets in 24 hours
  • do not use the maximum dosage for more than 2 weeks except under the advice and supervision of a doctor.

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 12 years of age and over: chew 2-4 tablets as symptoms occur, or as directed by a doctor
  • do not take for symptoms that persist for more than 2 weeks unless advised by a doctor

Other information

SPL UNCLASSIFIED SECTION

  • each tablet contains: elemental calcium 300mg
  • store below 30°C (86°F).Keep the container tightly closed

Inactive ingredients

INACTIVE INGREDIENT SECTION

adipic acid, blue 1, dextrose, flavors, magnesium stearate, maltodextrin, red 40, starch, sucralose, yellow 6, yellow 10.

Safety sealed: Do not use if printed seal under cap is torn or missing

Package/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 11673-615-90

Compare to TUMS® Smoothies Assorted Fruit*

extra strength

smooth dissolving antacid

calcium carbonate,750 mg

fast relief of heartburn, acid indigestion and upset stomach

ASSORTED FRUIT FLAVOR

90 TABLETS

90 CHEWABLE TABLETS

245 05 0761 R01 ID285492

Dist.by Target Corp.

Mpls.,MN 55403 Made in U.S.A

©2015 Target Brands, Inc.

Shop Target.com

Questions?Call 1-800-910-6874

*This product is not manufactured or distributed by GlaxoSmithKline, the distributor of TUMS®.


up and up extra strength smooth dissolving antacid assorted Fruit
up and up extra strength smooth dissolving antacid assorted Fruit

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
308915calcium carbonate 750 MG (Ca 300 MG) Chewable TabletPSN1
308915calcium carbonate 750 MG Chewable TabletSCD1
308915calcium carbonate 750 MG (calcium 300 MG) Chewable TabletSY1

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
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11673-615-902020-01-31C16284748780-19d75b9d0-ce20-f424-e053-dadaa90a57ceup and up extra strength smooth dissolving antacid

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11673-615-90up and up extra strength smooth dissolving antacidAssorted Fruit90 in 1 BOTTLE, PLASTICTABLET, CHEWABLE901

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-615UP AND UP EXTRA STRENGTH SMOOTH DISSOLVING ANTACID ASSORTED FRUIT (ANTACID TABLETS) TABLET, CHEWABLE [TARGET CORPORATION]1Legacy NDC, 1 package rows20160303_10e50d70-213b-4507-800f-fe308d0f7335.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11673-61511673-615-90

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
CALCIUM CARBONATEH0G9379FGKACTIB
ADIPIC ACID76A0JE0FKJIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
DEXTROSEIY9XDZ35W2IACT
MAGNESIUM STEARATE70097M6I30IACT
MALTODEXTRIN7CVR7L4A2DIACT
FD&C RED NO. 40WZB9127XOAIACT
STARCH, CORNO8232NY3SJIACT
SUCRALOSE96K6UQ3ZD4IACT
FD&C YELLOW NO. 6H77VEI93A8IACT
D&C YELLOW NO. 1035SW5USQ3GIACT

Source Document#

Source XML

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 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
10e50d70-213b-4507-800f-fe308d0f733510e50d70-213b-4507-800f-fe308d0f73352015-01-16WarningsExact identifier
spl id: 10e50d70-213b-4507-800f-fe308d0f7335
spl set id: 10e50d70-213b-4507-800f-fe308d0f7335

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.