UP AND UP POWDERLAX- polyethylene glycol 3350 powder, for solution

up and up powderlax by

Drug Labeling and Warnings

up and up powderlax by is a Otc medication manufactured, distributed, or labeled by Target Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each dose)

Polyethylene Glycol 3350, 17 g (cap filled to line)

Purpose

Osmotic Laxative

Use

• relieves occasional constipation (irregularity)
• generally produces a bowel movement in 1 to 3 days

Warnings

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

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

When using this product

you may have loose, watery, more frequent stools

Stop use and ask a doctor if

• you have rectal bleeding or your nausea, bloating, cramping or abdominal pain gets worse. These may be signs of a serious condition.
• you get diarrhea
• you need to use a laxative for longer 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. (1-800-222-1222)

Directions

• do not take more than directed unless advised by your doctor
• the bottle top is a measuring cap marked to contain 17 grams of powder when filled to the indicated line (white section in cap)
• adults and children 17 years of age and older:
• fill to top of white section in cap which is marked to indicate the correct dose (17 g)
• stir and dissolve in any 4 to 8 ounces of beverage (cold, hot or room temperature) then drink
• use once a day
• use no more than 7 days
• children 16 years of age or under: ask a doctor

Other information

• store at 20˚-25˚C (68˚-77˚F)
• tamper-evident: do not use if printed foil seal under cap is missing, open or broken

Inactive ingredients

none

Questions?

Call 1-888-547-7400

Principal Display Panel

Compare to active ingredient in MiraLAX®

powderlax®

polyethylene glycol 3350

powder for solution, osmotic laxative

relieves occasional constipation/irregularity

softens stool

unflavored powder

grit-free

14 DOSES

NET WT 8.3 OZ (238 g)

14 ONCE-DAILY DOSES

INGREDIENTS AND APPEARANCE

UP AND UP POWDERLAX 
polyethylene glycol 3350 powder, for solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-306
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P) (POLYETHYLENE GLYCOL 3350 - UNII:G2M7P15E5P)	POLYETHYLENE GLYCOL 3350	17 g  in 17 g

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11673-306-02	238 g in 1 BOTTLE; Type 0: Not a Combination Product	10/07/2009
2	NDC: 11673-306-03	510 g in 1 BOTTLE; Type 0: Not a Combination Product	10/07/2009
3	NDC: 11673-306-19	595 g in 1 BOTTLE; Type 0: Not a Combination Product	10/09/2013	02/03/2016
4	NDC: 11673-306-04	850 g in 1 BOTTLE; Type 0: Not a Combination Product	03/03/2014
5	NDC: 11673-306-17	289 g in 1 BOTTLE; Type 0: Not a Combination Product	08/27/2014	10/28/2016
6	NDC: 11673-306-09	765 g in 1 BOTTLE; Type 0: Not a Combination Product	10/21/2016
7	NDC: 11673-306-01	119 g in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2019
8	NDC: 11673-306-52	10 in 1 CARTON	04/11/2019
8		17 g in 1 PACKET; Type 0: Not a Combination Product
9	NDC: 11673-306-60	20 in 1 CARTON	04/11/2019
9		17 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA090685	10/07/2009

Labeler - Target Corporation (006961700)