FDA.reportPublic FDA data

Bio V Antacid Ultra Berry 72ct

Manufacturer
BioV Health Inc
Effective date
2024-04-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:10:40

Label at a glance#

ProductBio V Antacid Ultra Berry 72ct
Active ingredientCALCIUM CARBONATE
Label structure10 sections

Dosage and administration

adults and children 12 years of age and over: chew 2-3 tablets as symtoms occur, or as directed by a doctor do not take for symtoms 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 1000mg

Purpose

OTC - PURPOSE SECTION

Antacid

USE

INDICATIONS & USAGE SECTION

Relieves • acid indigestion • heartburn • 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 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 of reach of children

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 12 years of age and over:chew 2-3 tablets as symtoms occur, or as directed by a doctor
  • do not take for symtoms that persist for more than 2 weeks unless advised by a doctor 

Other information

SPL UNCLASSIFIED SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

FD&C Blue No.2 lake, FD&C Red No.40 lake, flavors, guar gum, hypromellose, magnesium stearate, sorbitol,  sucralose.

Questions or comments?

OTC - QUESTIONS SECTION

1-888-543-4199   

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
308892calcium carbonate 1000 MG (Ca 400 MG) Chewable TabletPSN2
308892calcium carbonate 1000 MG Chewable TabletSCD2
308892calcium carbonate 1000 MG (calcium 400 MG) Chewable TabletSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71481-007-012025-07-29C16284748780-11030e365-6628-111a-e063-dadaa90a10e2Bio V Antacid Ultra Berry Flavors
71481-007-012024-04-04C16284748780-11030e365-6628-111a-e063-dadaa90a10e2Bio V Antacid Ultra Berry Flavors
71481-007-012024-01-30C16284748780-11030e365-6628-111a-e063-dadaa90a10e2Bio V Antacid Ultra Berry Flavors

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71481-007-01Bio V Antacid Ultra Berry 72ct72 in 1 BOTTLETABLET722

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71481-007BIO V ANTACID ULTRA BERRY 72CT (CALCIUM CARBONATE) TABLET [BIOV HEALTH INC]2Legacy NDC, 1 package rows20240405_edf2033d-1271-4d6c-ada0-bbfc4d3ce2a3.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71481-00771481-007-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
FD&C BLUE NO. 2--ALUMINUM LAKE4AQJ3LG584IACT
FD&C RED NO. 40WZB9127XOAIACT
GUAR GUME89I1637KEIACT
HYPROMELLOSE, UNSPECIFIED3NXW29V3WOIACT
MAGNESIUM STEARATE70097M6I30IACT
SORBITOL506T60A25RIACT
SUCRALOSE96K6UQ3ZD4IACT
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
1549b584-d7b1-61d2-e063-6294a90ab148edf2033d-1271-4d6c-ada0-bbfc4d3ce2a32024-04-04WarningsExact identifier
spl id: 1549b584-d7b1-61d2-e063-6294a90ab148
spl set id: edf2033d-1271-4d6c-ada0-bbfc4d3ce2a3

Reported adverse events (FAERS/openFDA)#

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