Active Ingredient(s)

Anise Dry Extract 2%

Dry Fennel Extract 2%

Purpose

Light and Ease of Digestion

Use

Take 1 tablet 3-4 times a day when having issues with digestion

Warnings

No more than 6 tablets in a day.

Keep away from children

Do not use

in children less than 2 months of age
on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If any issues occur get medical help or contact a Poison Control Center right away.

Directions

Take 1 tablet 3-4 times a day.
Children under 12 years of age should not use product

Other information

Store between 15-30C (59-86F)
Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

Magnesium stearate, non-hydrogenated vegetable oil, Menthol, Star Asine essential oil,Stevia Powder

Package Label - Principal Display Panel

16 U NDC: 79394-000-01

DIGESTION-BLOATING-GAS
triplex pill

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:79394-000
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
FENNEL (UNII: 557II4LLC3) (FENNEL - UNII:557II4LLC3)	FENNEL	2 mg in 100 mg
ANISE OIL (UNII: 6Y89129C8H) (ANISE OIL - UNII:6Y89129C8H)	ANISE OIL	2 mg in 100 mg

Ingredient Name	Strength
Inactive Ingredients
STAR ANISE OIL (UNII: 6RXP35EIRE)
STEVIA LEAF (UNII: 6TC6NN0876)
MENTHOL (UNII: L7T10EIP3A)
MAGNESIUM STEARATE (UNII: 70097M6I30)
HYDROGENATED AVOCADO OIL (UNII: JA69U4B4XI)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	2mm
Flavor	ANISE	Imprint Code	TX
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:79394-000-01	24000 mg in 1 DOSE PACK; Type 0: Not a Combination Product	03/30/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		03/30/2020

Labeler - L'ENVOL PHARMA (362865293)

Registrant - L'ENVOL PHARMA (362865293)

Name	Address	ID/FEI	Business Operations
Establishment
L'ENVOL PHARMA		362865293	manufacture(79394-000)