UP AND UP POWDERLAX (POLYETHYLENE GLYCOL 3350) POWDER, FOR SOLUTION [TARGET CORPORATION]

UP AND UP POWDERLAX (POLYETHYLENE GLYCOL 3350) POWDER, FOR SOLUTION [TARGET CORPORATION]
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NDC 11673-306-01, 11673-306-02, 11673-306-03, 11673-306-04, 11673-306-09, 11673-306-17, 11673-306-19, 11673-306-52, 11673-306-60
Set ID 1bceb457-b24f-485d-bfe2-af4b7d38a5c2
Category HUMAN OTC DRUG LABEL
Packager Target Corporation
Generic Name
Product Class
Product Number
Application Number ANDA090685
  • 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
    ensure that the powder is fully dissolved before drinking
    do not drink if there are any clumps
    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 or comments?

    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

    7 DOSES

    NET WT 4.1 OZ (119 g) – 7 ONCE-DAILY DOSES

    powderlax image
  • INGREDIENTS AND APPEARANCE
    UP AND UP POWDERLAX 
    polyethylene glycol 3350 powder, for solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-306
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P) (POLYETHYLENE GLYCOL 3350 - UNII:G2M7P15E5P) POLYETHYLENE GLYCOL 335017 g  in 17 g
    Product Characteristics
    ColorWHITEScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-306-02238 g in 1 BOTTLE; Type 0: Not a Combination Product10/07/2009
    2NDC:11673-306-03510 g in 1 BOTTLE; Type 0: Not a Combination Product10/07/2009
    3NDC:11673-306-19595 g in 1 BOTTLE; Type 0: Not a Combination Product10/09/201302/03/2016
    4NDC:11673-306-04850 g in 1 BOTTLE; Type 0: Not a Combination Product03/03/201407/23/2019
    5NDC:11673-306-17289 g in 1 BOTTLE; Type 0: Not a Combination Product08/27/201410/28/2016
    6NDC:11673-306-09765 g in 1 BOTTLE; Type 0: Not a Combination Product10/21/2016
    7NDC:11673-306-01119 g in 1 BOTTLE; Type 0: Not a Combination Product04/12/2019
    8NDC:11673-306-5210 in 1 CARTON04/11/201911/01/2020
    817 g in 1 PACKET; Type 0: Not a Combination Product
    9NDC:11673-306-6020 in 1 CARTON04/11/201912/01/2020
    917 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA09068510/07/2009
    Labeler - Target Corporation (006961700)