Label: UP AND UP POWDERLAX- polyethylene glycol 3350 powder, for solution
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NDC Code(s):
11673-306-01,
11673-306-02,
11673-306-03,
11673-306-04, view more11673-306-09, 11673-306-17, 11673-306-19, 11673-306-52, 11673-306-60
- Packager: Target Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated February 15, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each dose)
- Purpose
- Use
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Warnings
Allergy alert: Do not use if you are allergic to polyethylene glycol
Ask a doctor before use if you have
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- nausea, vomiting or abdominal pain
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- a sudden change in bowel habits that lasts over 2 weeks
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- irritable bowel syndrome
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Directions
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- do not take more than directed unless advised by your doctor
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- the bottle top is a measuring cap marked to contain 17 grams of powder when filled to the indicated line (white section in cap)
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- adults and children 17 years of age and older:
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- use once a day
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- fill to top of white section in cap which is marked to indicate the correct dose (17 g)
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- stir and dissolve in any 4 to 8 ounces of beverage (cold, hot or room temperature) then drink
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- do not combine with starch-based thickeners used for difficulty swallowing
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- ensure that the powder is fully dissolved before drinking
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- do not drink if there are any clumps
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- do not use more than 7 days
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- children 16 years of age or under: ask a doctor
- Other information
- Inactive ingredients
- Questions or comments?
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
UP AND UP POWDERLAX
polyethylene glycol 3350 powder, for solutionProduct 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 07/23/2019 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 11/01/2020 8 17 g in 1 PACKET; Type 0: Not a Combination Product 9 NDC:11673-306-60 20 in 1 CARTON 04/11/2019 12/01/2020 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)