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)
- Purpose
- Use
-
Warnings
Allergy alert: Do not use if you are allergic to polyethylene glycol
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
-
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
- Inactive ingredients
- Questions or comments?
- Principal Display Panel
-
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)