Your browser does not support JavaScript! EZ2GO (POLYETHYLENE GLYCOL 3350) POWDER [VALLEY MEDICAL PRODUCTS,LLC]
DailyMed Logo Header image

Daily Med

Current Medication Information


RxNorm Names

EZ2GO (polyethylene glycol 3350) powder
[Valley Medical Products,LLC]

Category DEA Schedule Marketing Status
HUMAN OTC DRUG LABEL Abbreviated New Drug Application
Drug Label Sections

Inactive Ingredients   none

Active Ingredient

Polyethylene Glycol 3350, 17 g


Osmotic Laxative


Allergy Alert: Do not use if you are allergic to polyethylene glycol

Do not use if you have kidney disease, except under the advice and supervision of a doctor

When using this product, you may have loose, watery, more frequent stools

Ask a doctor before use if you have

-nausea, vomiting or abdominal pain

-a sudden change in bowel habits that lasts over 2 weeks

-irritable bowel syndrome

Ask a doctor or pharmacist before use if you are taking a prescription drug

Stop use and ask a doctor if

- you have rectal bleeding or your nausea, bloating, cramping or abdominal pain gets worse.These may be sogns of a serious condition.

- you get diarrhea

- you need to use a laxative for longer than 1 week

- side effects may occur. you may report the side effects

to FDA at 1 - 800 - FDA - 1088

Keep out of reach of children. In case of overdose, get medical help or contact a POISON CONTROL CENTER  right away.

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


-do not take more than directed unless advised by your doctor

-adults and children 17 years of age and older:

    -stir and dissolve one packet (17g) in any 4 to 8 ounces of beverage  (cold, hot or room temperature) and then drink

    -use once a day

    -use no more than 7 days

-Children 16 years of age or under:  ask a doctor

Questions or comments?



-relieves occasional constipation (irregularity)

-generally produces a bowel movement in 1 to 3 days

copy of label

polyethylene glycol 3350 powder
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:76470-005
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76470-005-05238 g in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Labeler - Valley Medical Products,LLC (969389407)
NameAddressID/FEIBusiness Operations
Valley Medical Products,LLC969389407relabel(76470-005), repack(76470-005)
NameAddressID/FEIBusiness Operations
Novel Laboratories, Inc.793518643manufacture(76470-005)

Revised: 9/2013
Valley Medical Products,LLC

Visit The National Library of Medicine Copyright, Privacy, Accessibility
U.S. National Library of Medicine, 8600 Rockville Pike, Bethesda, MD 20894
National Institutes of Health, Health & Human Services