FEVIA CONSTIPATION CONTROL- docusate sodium capsule, liquid filled

FEVIA Constipation Control by

Drug Labeling and Warnings

FEVIA Constipation Control by is a Otc medication manufactured, distributed, or labeled by VIVUNT PHARMA LLC, MEDGEL PRIVATE LIMITED. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients (in each softgel)

• Docusate sodium 100 mg

Purpose

• Stool softener laxative

Uses

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

Warnings

Warnings

Do not use

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

Ask a doctor before use if you have

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

Stop use and ask a doctor if

• 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

• 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,

ask a health professional before use.

Keep out of reach of children

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

Directions

• 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

Other 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

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.

Questions?

Visit www.fevia.live/contact

Distributed by

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

FEVIA™

CONSTIPATION CONTROL

Stool Softener

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

INGREDIENTS AND APPEARANCE

FEVIA CONSTIPATION CONTROL 
docusate sodium capsule, liquid filled

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82706-029
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG)	DOCUSATE SODIUM	100 mg

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
GELATIN (UNII: 2G86QN327L)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
FD&C RED NO. 40 (UNII: WZB9127XOA)
POVIDONE K30 (UNII: U725QWY32X)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SORBITOL SOLUTION 70% (UNII: 8KW3E207O2)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	red (transparent)	Score	no score
Shape	OVAL	Size	5mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82706-029-01	1 in 1 CARTON	02/19/2026
1		50 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M007	02/19/2026

Labeler - VIVUNT PHARMA LLC (045829437)

Establishment
Name	Address	ID/FEI	Business Operations
MEDGEL PRIVATE LIMITED		677385498	manufacture(82706-029)