up and up extra strength smooth dissolving antacid

Manufacturer
Target corporation
Effective date
2025-11-04
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 01:42:05

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 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 at room temperature. 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

Questions

OTC - QUESTIONS SECTION

1-866-467-2748

Package/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Compare to active ingredient in TUMS ®Smoothies*

extra strength

smooth dissolving antacid

calcium carbonate, 750 mg

fast relief of heartburn, acid indigestion and upset stomach

ASSORTED FRUIT FLAVOR

GLUTEN-FREE

245 05 0385 R00 IDC-000450-01-057

245 05 0613 R00 C-000974-01-012

Dist.by Target Corp.

Mpls., MN 55403

Made in U.S.A

©2017 Target Brands, Inc.

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

Package Label for 60 Chewable Tablets

up and up extra strength amooth dissolving 60 chewable tablets
up and up extra strength amooth dissolving 60 chewable tablets

Package Label for 140 Chewable Tablets

SPL UNCLASSIFIED SECTION

Up and Up extra strength antacid 140 chewable tablets
Up and Up extra strength antacid 140 chewable tablets

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
308915calcium carbonate 750 MG (Ca 300 MG) Chewable TabletPSN8
308915calcium carbonate 750 MG Chewable TabletSCD8
308915calcium carbonate 750 MG (calcium 300 MG) Chewable TabletSY8

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130368163115628GTIN-13: 0368163115628
EAN-13: 0368163115628
GTIN-12: 368163115628
UPC-A: 368163115628
GTIN storage (14 digits): 00368163115628
103AF72PVLFLB.jpg

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
11673-715-40up and up extra strength smooth dissolving antacidAssorted Fruit140 in 1 BOTTLE, PLASTICTABLET, CHEWABLE1408
11673-715-60up and up extra strength smooth dissolving antacidAssorted Fruit60 in 1 BOTTLE, PLASTICTABLET, CHEWABLE608

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11673-71511673-715-60, 11673-715-40

Ingredients#

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

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

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
72024-11-07full-release2026-06-01 00:35:55

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
up and up extra strength smooth dissolving antacid Assorted FruitCALCIUM CARBONATETarget corporationb97558c5-d836-42ae-bfa5-0f4c6bca7e4a2025-11-04WarningsExact identifier
ndc (package): 11673-715-40
ndc (package): 11673-715-60
ndc (product): 11673-715
ndc11 (package): 11673071540
ndc11 (package): 11673071560
spl id: 42c2e2f5-2828-66d4-e063-6394a90a9af9
spl set id: b97558c5-d836-42ae-bfa5-0f4c6bca7e4a

Reported adverse events (FAERS/openFDA)#

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