RITE AID Ultra Strength Antacid Tablets Drug Facts

Manufacturer
RITE AID CORPORATION
Effective date
2024-10-30
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 00:32:22

Label at a glance#

ProductRite Aid Ultra Strength Assorted Berries
Active ingredientCALCIUM CARBONATE
Label structure10 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 2-3 tablets completely 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

Storage and handling

• each tablet contains: elemental calcium 400mg • Store at room temperature. Keep the container tightly closed.

Label contents#

Full prescribing information#

Active ingredient (per tablet)

OTC - ACTIVE INGREDIENT SECTION

Calcium Carbonate USP 1000 mg

Purpose

OTC - PURPOSE SECTION

Antacid

Uses

INDICATIONS & USAGE SECTION

relieves

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

Ask a doctor or pharmacist before use if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

presently taking a prescription drug. Antacids may interact with certain prescription drugs.

When using this product

OTC - WHEN USING SECTION

  • do not take more than 7 tablets in 24 hours
  • if pregnant do not take more than 5 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 2-3 tablets completely 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

STORAGE AND HANDLING SECTION

  • each tablet contains: elemental calcium 400mg
  • Store at room temperature. Keep the container tightly closed.

Inactive ingredients

INACTIVE INGREDIENT SECTION

adipic acid, dextrose, FD&C Blue No. 1, FD&C Red No. 40, flavors, magnesium stearate, maltodextrin, starch, sucralose.

Questions or comments?

OTC - QUESTIONS SECTION

1-866-467-2748

Safety Sealed

OTC - DO NOT USE SECTION

DO NOT USE IF PRINTED SEAL UNDER CAP IS TORN OR MISSING

Package/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

RITE AID PHARMACY®

Compare to the active ingredient Ultra Strength Tums®

ULTRA STRENGTH

antacid

calcium carbonate 1000 mg

assorted berries flavor

naturally and artificially flavored

fast relief of upset stomach, heartburn and acid indigestion.

K PAREVE

72 CHEWABLE TABLETS

GLUTEN FREE

DISTRIBUTED BY:

RITE AID, 30 HUNTER LANE,

CAMP HILL, PA 17011

www.riteaid.com

IF YOU ARE NOT SATISFIED, WE’LL HAPPILY REFUND YOUR MONEY.

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

Rite Aid Assorted Berry 72 Chewable Tablets
Rite Aid Assorted Berry 72 Chewable Tablets

Ultra Strength 160 Chewable Label

SPL UNCLASSIFIED SECTION

Ultra Strength Antacid Assorted Berry 160 Chewable Tablets
Ultra Strength Antacid Assorted Berry 160 Chewable Tablets

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
308892calcium carbonate 1000 MG (Ca 400 MG) Chewable TabletPSN8
308892calcium carbonate 1000 MG Chewable TabletSCD8
308892calcium carbonate 1000 MG (calcium 400 MG) Chewable TabletSY8

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
11822-1037-1Rite Aid Ultra StrengthAssorted Berries160 in 1 BOTTLETABLET, CHEWABLE1608
11822-1037-2Rite Aid Ultra StrengthAssorted Berries72 in 1 BOTTLETABLET, CHEWABLE728

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-1037RITE AID ULTRA STRENGTH ASSORTED BERRIES (CALCIUM CARBONATE) TABLET, CHEWABLE [RITE AID CORPORATION]8Current NDC, Legacy NDC, 2 package rows20241101_ea918cb1-af3e-4a02-bd34-db4ad1b0e6bd.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11822-103711822-1037-1, 11822-1037-2

Ingredients#

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

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

Source Document#

Source XML · Source PDF

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
Rite Aid Ultra Strength Assorted BerriesCALCIUM CARBONATERITE AID CORPORATIONea918cb1-af3e-4a02-bd34-db4ad1b0e6bd2024-10-30WarningsExact identifier
ndc (package): 11822-1037-2
ndc (package): 11822-1037-1
ndc (product): 11822-1037
ndc11 (package): 11822103701
ndc11 (package): 11822103702
spl id: ee63f4ae-cad5-4094-a012-2daa98c0ccef
spl set id: ea918cb1-af3e-4a02-bd34-db4ad1b0e6bd

Reported adverse events (FAERS/openFDA)#

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