FDA.reportPublic FDA data

Genexa Antacid

Manufacturer
Genexa Inc.
Effective date
2025-02-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:54:44

Label at a glance#

ProductGenexa Antacid Maximum Strength
Active ingredientCALCIUM CARBONATE
Label structure11 sections

Storage and handling

Other information each tablet contains: elemental calcium 400 mg store between 20-25°C (68-77°F) in a dry place out of direct sunlight

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each tablet)

Calcium carbonate USP 1000 mg

OTC - PURPOSE SECTION

Purpose

Antacid

INDICATIONS & USAGE SECTION

Uses relieves

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

WARNINGS SECTION

Warnings

OTC - ASK DOCTOR/PHARMACIST SECTION

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

OTC - WHEN USING SECTION

When using this product

  • 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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

DOSAGE & ADMINISTRATION SECTION

Directions

adults and children 12 years of age and over: chew 2-3 tablets as symptoms occur, or as directed by a doctor

STORAGE AND HANDLING SECTION

Other information

  • each tablet contains: elemental calcium 400 mg
  • store between 20-25°C (68-77°F) in a dry place out of direct sunlight

INACTIVE INGREDIENT SECTION

Inactive ingredients organic beet root, organic carnauba wax, non-GMO dextrose, organic flavors, organic maltodextrin, organic rice bran extract

OTC - QUESTIONS SECTION

Questions?1-855-436-3921

SPL UNCLASSIFIED SECTION

Tamper evident: Do not use if bottle seal under the cap is disturbed or missing.

*This product is not manufactured or distributed by GlaxoSmithKline Consumer Healthcare (US) Private LLC, owner of the registered trademark TUMS® Ultra Strength 1000 Assorted Berries.

Patent Pending | Distributed by: Genexa Inc., Atlanta, GA 30324 | genexa.com

Made in the USA with globally sourced ingredients

NDC 69676-0072-4

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Genexa®

MEDICINE MADE CLEAN

Antacid Maximum Strength

Calcium Carbonate 1000 mg

Heartburn

Acid Indigestion

Upset Stomach

Compare to active ingredient in TUMS® Ultra Strength 1000 Assorted Berries*

Medicine made clean

Same effective active ingredient, but no artificial fillers.

Organic Berry & Vanilla Flavor

72 Chewable Tablets

16A_Label_R-20240412_Page_116A_Label_R-20240412_Page_1

16A_Back Label_R-2024041216A_Back Label_R-20240412

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
308892calcium carbonate 1000 MG (Ca 400 MG) Chewable TabletPSN3
308892calcium carbonate 1000 MG Chewable TabletSCD3
308892calcium carbonate 1000 MG (calcium 400 MG) Chewable TabletSY3

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69676-0072-42025-02-07C16284748780-12cef2736-7276-d83d-e063-dadaa90ab31fAntacid Maximum Strength
69676-0072-42025-01-30C16284748780-12cef2736-7276-d83d-e063-dadaa90ab31fAntacid Maximum Strength

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69676-0072-4Genexa AntacidMaximum Strength72 in 1 BOTTLETABLET, CHEWABLE723

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69676-0072GENEXA ANTACID MAXIMUM STRENGTH (CALCIUM CARBONATE) TABLET, CHEWABLE [GENEXA INC.]3Current NDC, Legacy NDC, 1 package rows20250210_e4b8f068-ad52-10c8-e053-2a95a90a871f.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69676-007269676-0072-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
BEETN487KM8COKIACT
CARNAUBA WAXR12CBM0EIZIACT
DEXTROSEIY9XDZ35W2IACT
MALTODEXTRIN7CVR7L4A2DIACT
RICE BRANR60QEP13ICIACT
CALCIUM CARBONATEH0G9379FGKACTIB

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
Genexa Antacid Maximum StrengthCALCIUM CARBONATEGenexa Inc.e4b8f068-ad52-10c8-e053-2a95a90a871f2025-02-07WarningsExact identifier
ndc (package): 69676-0072-4
ndc (product): 69676-0072
ndc11 (package): 69676007204
spl id: 2d97d533-ee09-3bf8-e063-6294a90ab895
spl set id: e4b8f068-ad52-10c8-e053-2a95a90a871f

Reported adverse events (FAERS/openFDA)#

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