FDA.reportPublic FDA data

up and up extra strength antacid 750

Manufacturer
Target Corporation
Effective date
2025-11-04
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 01:41:57

Label at a glance#

Productup and up extra strength antacid 750 Assorted Berry
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 arepresently taking 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).

Inactive ingredients

INACTIVE INGREDIENT SECTION

adipic acid, blue 1 lake, dextrose, flavors, magnesium stearate, maltodextrin, red 40 lake, starch, sucralose.

Questions?

OTC - QUESTIONS SECTION

1-866-467-2748

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 11673-902-24

Compare to Tums® Extra Strength*

extra strength

antacid 750

calcium carbonate

relief of heartburn, acid indigestion, sour stomach and upset stomach associated with these symptoms

ASSORTED BERRY FLAVOR

96 CHEWABLE TABLETS

Naturally and artificially flavored

GLUTEN FREE

245 05 0459 R00

IDC-000274-01-007

Dist. by Target Corp.

Mpls., MN 55403

©2016 Target Brands, Inc.

*This product is not manufactured or distributed by GlaxoSmithKline LLC, owner of the registered trademark Tums®.

up and up extra strength antacid 750 Chewable Tablet
up and up extra strength antacid 750 Chewable Tablet

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
308915calcium carbonate 750 MG (Ca 300 MG) Chewable TabletPSN9
308915calcium carbonate 750 MG Chewable TabletSCD9
308915calcium carbonate 750 MG (calcium 300 MG) Chewable TabletSY9

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CALCIUM CATION Pharmacologic Class Indexing3Indexing - Pharmacologic Class20230427

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11673-902-24up and up extra strength antacid 750Assorted Berry96 in 1 BOTTLE, PLASTICTABLET, CHEWABLE969

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11673-90211673-902-24

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ADIPIC ACID76A0JE0FKJIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
DEXTROSE, UNSPECIFIED FORMIY9XDZ35W2IACT
MAGNESIUM STEARATE70097M6I30IACT
MALTODEXTRIN7CVR7L4A2DIACT
FD&C RED NO. 40WZB9127XOAIACT
STARCH, CORNO8232NY3SJIACT
SUCRALOSE96K6UQ3ZD4IACT
CALCIUM CARBONATEH0G9379FGKACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
82024-11-07full-release2026-06-01 00:35:34

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
up and up extra strength antacid 750 Assorted BerryANTACID TABLETSTarget Corporation46f11acf-a968-4fdd-8755-3eff0b9b67d02025-11-04WarningsExact identifier
ndc (package): 11673-902-24
ndc (product): 11673-902
ndc11 (package): 11673090224
spl id: 42c1ffe8-3aa8-7211-e063-6394a90acee9
spl set id: 46f11acf-a968-4fdd-8755-3eff0b9b67d0
up and up extra strength antacid 750 Assorted BerryANTACID TABLETSTarget Corporationb76441ad-f701-4d0d-b9a7-18ac466faa442025-11-04WarningsExact identifier
ndc (product): 11673-902

Reported adverse events (FAERS/openFDA)#

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