Drug Facts

Drug Labeling and Warnings

Drug Details [pdf]

EZ2GO - bisacodyl pill 
Valley Medical Products,LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active Ingredients

(In each tablet)

Bisacodyl USP 5 mg


Purpose

Stimulant Laxative


Warnings

Do not use if you cannot swallow without chewing

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

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 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.

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


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 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 Ingredients

Calcium Carbonate, Dicalcium Phospate,

Cellulose, Stearic Acid, Maltodextrin,

Croscarmellose Sodium, Pharmaceutical

Glaze, Magnesium Stearate, Silicon

Dioxide, Carnauba Wax

copy of label

EZ2GO  
bisacodyl pill
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 76470-010
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BISACODYL (UNII: 10X0709Y6I) (DEACETYLBISACODYL - UNII:R09078E41Y) BISACODYL5 mg  in 5 mg
Inactive Ingredients
Ingredient NameStrength
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
ColorwhiteScoreno score
ShapeROUNDSize6mm
FlavorImprint Code TCLover003
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 76470-010-1010 mg in 1 POUCH; Type 0: Not a Combination Product01/01/201505/31/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33401/01/201505/31/2019
Labeler - Valley Medical Products,LLC (969389407)
Establishment
NameAddressID/FEIBusiness Operations
Valley Medical Products,LLC969389407repack(76470-010) , relabel(76470-010)

Revised: 6/2019