EZ2GO - polyethylene glycol 3350 powder 
Valley Medical Products,LLC


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 Type HUMAN OTC DRUG Item Code (Source) NDC:76470-005
Route of Administration ORAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:76470-005-05 238 g in 1 BOTTLE; Type 0: Not a Combination Product 10/20/2012
2 NDC:76470-005-17 17 g in 1 POUCH; Type 0: Not a Combination Product 10/20/2012
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA091077 10/20/2012
Labeler - Valley Medical Products,LLC (969389407)
Name Address ID/FEI Business Operations
Valley Medical Products,LLC 969389407 relabel(76470-005) , repack(76470-005)
Name Address ID/FEI Business Operations
Novel Laboratories, Inc. 793518643 manufacture(76470-005)

Revised: 1/2017
Document Id: 44501029-845e-4428-a6b0-4031c6bfdc58
Set id: e3d5058d-7575-482a-ba33-3498ac61240a
Version: 2
Effective Time: 20170127
Valley Medical Products,LLC