EZ2GO- dimethicone tablet, chewable

ez2go by

Drug Labeling and Warnings

ez2go by is a Otc medication manufactured, distributed, or labeled by Valley Medical Products,LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INACTIVE INGREDIENT

Inactive Ingredients  compressible sugar, dextrose, flavor,

magnesium stearate, maltodextirn, microcrystalline

cellulose, sorbitol.

ACTIVE INGREDIENT

Active Ingredient (in each tablet)

Simethicone 80 mg

PURPOSE

Purpose

Antigas

INDICATIONS & USAGE

Uses - relieves -pressure - bloating

-symptoms referred to as gas

KEEP OUT OF REACH OF CHILDREN

Warnings  Keep out of the reach of children.

WARNINGS

Warnings  Keep out of the reach of children. In case of overdose,

get medical help or contact a Poison Control Center

immediately.

DOSAGE & ADMINISTRATION

Directions

-chew 2 to 4 tablets thoroughly as needed

after meals and at bedtime

-do not exceed 6 tablets per day

unless directed by a physician

STORAGE AND HANDLING

Other Information

-do not use if inner seal is broken

-store at room temperature

-avoid high humidity and excessive heat,

above 40 C (104 F)

QUESTIONS

Qiestions or Comments?

800-403-9832 or www.ez2go.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EZ2GO 
dimethicone tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76470-012
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O)	DIMETHICONE	80 mg  in 80 mg

Inactive Ingredients
Ingredient Name	Strength
SUCROSE (UNII: C151H8M554)
DEXTROSE (UNII: IY9XDZ35W2)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
SORBITOL (UNII: 506T60A25R)

Product Characteristics
Color	white (white)	Score	no score
Shape	ROUND	Size	13mm
Flavor		Imprint Code	GPI;LB
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76470-012-12	80 mg in 1 POUCH; Type 0: Not a Combination Product	01/01/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part332	01/01/2015

Labeler - Valley Medical Products,LLC (969389407)

Establishment
Name	Address	ID/FEI	Business Operations
Guardian Drug Company		119210276	manufacture(76470-012)

Establishment
Name	Address	ID/FEI	Business Operations
Valley Medical Products,LLC		969389407	repack(76470-012) , relabel(76470-012)