EZ2go by Valley Medical Products,LLC EZ2GO- bisacodyl pill

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]

ACTIVE INGREDIENT

Active Ingredients

(In each tablet)

Bisacodyl USP 5 mg

PURPOSE

Purpose

Stimulant Laxative

WARNINGS

Warnings

Do not use if you cannot swallow without chewing

ASK DOCTOR

Ask a doctor before use if you have

Stomach pain, nausea or bleeding

A sudden change in bowel habits that lasts more than 2 weeks

INDICATIONS & USAGE

Uses

-For temporary relief of occasional

constipation and irregularity

Generally produces a bowel movement

in 6 to 12 hours

When using this product

Do not chew or cush tablet(s)

Do not use within 1 hour after taking an antacid  or milk

It may cause stomach discomfort, faintness and cramps

STOP USE

Stop use and ask 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

If pregnant or breast-feeding, ask a health professional before use

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions

Take with a glass of water

Adults and children 12 years of age and over: 1 to 3 tablets in a single daily dose.

Children 6 to 12 years of age: 1 tablet in a single daily use.

OTHER SAFETY INFORMATION

Other information:

Store at 20-25 C (68-77 F)

Protect from excessive humidity

Packaged for your protection.

Do not use if individual seals are broken.

INACTIVE INGREDIENT

Inactive Ingredients

Calcium Carbonate, Dicalcium Phospate,

Cellulose, Stearic Acid, Maltodextrin,

Croscarmellose Sodium, Pharmaceutical

Glaze, Magnesium Stearate, Silicon

Dioxide, Carnauba Wax

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EZ2GO  
bisacodyl pill

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76470-011
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BISACODYL (UNII: 10X0709Y6I) (DEACETYLBISACODYL - UNII:R09078E41Y)	BISACODYL	5 mg  in 5 mg

Inactive Ingredients
Ingredient Name	Strength
CALCIUM CARBONATE (UNII: H0G9379FGK)
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: L11K75P92J)
POWDERED CELLULOSE (UNII: SMD1X3XO9M)
STEARIC ACID (UNII: 4ELV7Z65AP)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
SHELLAC (UNII: 46N107B71O)
MAGNESIUM STEARATE (UNII: 70097M6I30)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
CARNAUBA WAX (UNII: R12CBM0EIZ)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	6mm
Flavor		Imprint Code	TCLover003
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76470-011-11	20 mg in 1 BOTTLE; 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 not final	part334	01/01/2015

Labeler - Valley Medical Products,LLC (969389407)

Establishment
Name	Address	ID/FEI	Business Operations
LNK International, Inc.		038154464	pack(76470-011)

Establishment
Name	Address	ID/FEI	Business Operations
LNK International, Inc.		832867837	pack(76470-011)

Establishment
Name	Address	ID/FEI	Business Operations
LNK International, Inc.		967626305	pack(76470-011)

Establishment
Name	Address	ID/FEI	Business Operations
Valley Medical Products,LLC		969389407	repack(76470-011) , relabel(76470-011)