FDA.reportPublic FDA data

Fevia Constipation Control 50

Manufacturer
VIVUNT PHARMA LLC | MEDGEL PRIVATE LIMITED
Effective date
2026-07-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-07-21 05:10:13

Label at a glance#

ProductFEVIA Constipation Control
Active ingredientDOCUSATE SODIUM
Label structure10 sections

Indications and uses

for relief of occasional constipation and irregularity this product generally produces bowel movement in 12 to 72 hour

Dosage and administration

Take with a glass of water adults and children 12 years and over (may be taken as a single daily ose or in divided dose) 1 or 3 softgels children 2 to under 12 years 1 softgel daily children under 2 years ask a doctor

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredients (in each softgel)

  • Docusate sodium 100 mg

Purpose

OTC - PURPOSE SECTION

  • Stool softener laxative

Uses

INDICATIONS & USAGE SECTION

  • for relief of occasional constipation and irregularity
  • this product generally produces bowel movement in 12 to 72 hour

Warnings

WARNINGS SECTION

Warnings

Do not use

OTC - DO NOT USE SECTION

  • If you are presently taking mineral oil, unless told to do so by a doctor

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • stomach pain, nausea or vomiting
  • a sudden change in bowel habits that lasts more than 2 weeks.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • you have rectal bleeding or no bowel movement after using this product. These could be signs of a serious condition.
  • you need to use a laxative for more than 1 week.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • you have rectal bleeding or no bowel movement after using this prodct. These could be signs of a serious condition.
  • you need to use a laxative for more than 1 week.

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

In case of overdose, get Control Center (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Take with a glass of water
adults and children 12 years and over (may be taken as a single daily ose or in divided dose)1 or 3 softgels
children 2 to under 12 years1 softgel daily
children under 2 yearsask a doctor

Other information

OTHER SAFETY INFORMATION

  • Each softgel contains: sodium 0.005 mg
  • Store at 20-25°C (68-77°F)
  • Protect from light, heat and moisture
  • Contains FD&C Yellow No.6

Inactive ingredients

INACTIVE INGREDIENT SECTION

FD&C Red No. 40, FD&C Yellow No.6, Gelatin, Glycerin, Polyethylene Glycol, Povidone PVPK-30, Propylene glycol, Purified water, Sorbitol 70% Solution, Titanium dioxide.

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

Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FEVIA™

Constipation Control

Stool Softener

Goes to work in minutes

Docusate Sodium 100 mg

50 SOFTGELS

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

Stimulant Free

Easy to swallow softgels

Actual size

PDPPDP

PDP interiorPDP interior

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130850047780713GTIN-13: 0850047780713
EAN-13: 0850047780713
GTIN-12: 850047780713
UPC-A: 850047780713
GTIN storage (14 digits): 00850047780713		CONSTIPATION CONTROL box.jpg

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
82706-02982706-029-01

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
GLYCERINPDC6A3C0OXIACT
GELATIN2G86QN327LIACT
FD&C YELLOW NO. 6H77VEI93A8IACT
FD&C RED NO. 40WZB9127XOAIACT
POVIDONE K30U725QWY32XIACT
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SORBITOL SOLUTION 70%8KW3E207O2IACT
DOCUSATE SODIUMF05Q2T2JA0ACTIB
POLYETHYLENE GLYCOL, UNSPECIFIED3WJQ0SDW1AIACT
TITANIUM DIOXIDE15FIX9V2JPIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22026-02-27full-release2026-06-01 01:47:44
12026-02-18monthly-update2026-06-03 17:56:43

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
FEVIA Constipation ControlDOCUSATE SODIUMVIVUNT PHARMA LLC4b21ca11-b81f-402c-e063-6394a90a3acb2026-07-15WarningsExact identifier
ndc (package): 82706-029-01
ndc (product): 82706-029
ndc11 (package): 82706002901
spl id: 56afa52d-5dfb-9360-e063-6294a90af27d
spl set id: 4b21ca11-b81f-402c-e063-6394a90a3acb

Reported adverse events (FAERS/openFDA)#

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