FDA.reportPublic FDA data

FEVIA Acid Control 60

Manufacturer
VIVUNT PHARMA LLC | FINECURE PHARMACEUTICALS LIMITED
Effective date
2026-07-15
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
daily-update
Hydrated at
2026-07-21 05:10:11

Label at a glance#

ProductFEVIA Acid Control
Active ingredientCALCIUM CARBONATE
Label structure10 sections

Indications and uses

relieves: acid indigestion sour stomach heartburn upset stomach associate with these symptoms

Dosage and administration

adult and children 12 years of age and over: chew 2-3 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. These could be signs of a serious condition.

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredients (in each tablet)

Calcium Carbonate 1000 mg

Purpose

OTC - PURPOSE SECTION

  • Antacid

Uses

INDICATIONS & USAGE SECTION

relieves:

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

Warnings

WARNINGS SECTION

Warnings

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

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

When using this product

OTC - WHEN USING SECTION

  • do not takemore than 6 tablets in a 24 - hour period

do not use

OTC - DO NOT USE SECTION

  • the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a physician

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

  • adult and children 12 years of age and over: chew 2-3 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. These could be signs of a serious condition.

Other information

OTHER SAFETY INFORMATION

  • Each chewable tabet contains:elemental calcium 400 mg, sodium 1 mg
  • Store below 30°C (86°F)
  • Protect from light, heat and moisture

Inactive ingredients

INACTIVE INGREDIENT SECTION

Adipic acid, Corn starch, FD&C Blue No.1 Aluminum lake, FD&C Red No.40 Aluminum lake, Flavors, Magnesium stearate, Maltodextrin, Mineral oil, Sodium polyphospate, Sucrose, Talc.

Distributed by

SPL UNCLASSIFIED SECTION

VIVUNT

Distributed by: VIVUNT PHARMA LLC

8950 SW 74th Court, Suite 1901

Miami, FL 33156-3178, USA.

Product from India.

www.vivunt.live

Pakage PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FEVIA™

Acid Control

Antacid

Relieve acid pain instantly

Calcium Carbonate 1000 mg

ASSORTED BERRIES

60 CHEWABLE TABLET

TAMPER EVIDENT: DO NOT USE IF CARTON IS OPEN OR IF SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

Chewable - No Water Needed

Actual size

PDPPDP

PDP interiorPDP interior

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

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
82706-02782706-027-02

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
MALTODEXTRIN7CVR7L4A2DIACT
FD&C BLUE NO. 1 ALUMINUM LAKEJ9EQA3S2JMIACT
FD&C RED NO. 40 ALUMINUM LAKE6T47AS764TIACT
MAGNESIUM STEARATE70097M6I30IACT
STARCH, CORNO8232NY3SJIACT
SODIUM POLYMETAPHOSPHATEP1BM4ZH95LIACT
SUCROSEC151H8M554IACT
ADIPIC ACID76A0JE0FKJIACT
TALC7SEV7J4R1UIACT
MINERAL OILT5L8T28FGPIACT
CALCIUM CARBONATEH0G9379FGKACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42026-03-19full-release2026-06-01 01:50:44
12026-02-18monthly-update2026-06-03 17:56:46

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
FEVIA Acid ControlCALCIUM CARBONATEVIVUNT PHARMA LLC4b1bd2d1-c909-f5db-e063-6394a90a84bc2026-07-15WarningsExact identifier
ndc (package): 82706-027-02
ndc (product): 82706-027
ndc11 (package): 82706002702
spl id: 56af3d98-942a-3403-e063-6294a90a5172
spl set id: 4b1bd2d1-c909-f5db-e063-6394a90a84bc
FEVIA Acid ControlCALCIUM CARBONATEVIVUNT PHARMA LLC4d695a90-6502-3020-e063-6394a90ab0c32026-07-15WarningsExact identifier
ndc (product): 82706-027

Reported adverse events (FAERS/openFDA)#

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