Up and Up Naproxen Sodium
Name: Up and Up Naproxen Sodium
Purpose
Pain reliever/fever reducer
Directions
- do not take more than directed
- the smallest effective dose should be used
- do not take longer than 10 days, unless directed by a doctor (see Warnings)
- drink a full glass of water with each dose
| Adults and children 12 years and older | - take 1 tablet every 8 to 12 hours while symptoms last
- for the first dose you may take 2 tablets within the first hour
- do not exceed 2 tablets in any 8- to 12-hour period
- do not exceed 3 tablets in a 24-hour period
|
| Children under 12 years | |
Questions?
Principal Display Panel
Naproxen Sodium Tablets, 220 mg
Pain Reliever/Fever Reducer (NSAID)
Compare to active ingredient in Aleve® Tablets
See New Warnings Information
8 to 12 hour dosing
# Tablets (insert # of tables in package in place of "#")
Shown Actual Size Above
Naproxen Sodium Tablets, 220 mg Carton
Up and Up Naproxen Sodium naproxen sodium tablet |
| Product Information | | Product Type | HUMAN OTC DRUG | Item Code (Source) | NDC:11673-490 | | Route of Administration | ORAL | DEA Schedule | | |
| Active Ingredient/Active Moiety | | Ingredient Name | Basis of Strength | Strength | | NAPROXEN SODIUM (NAPROXEN) | NAPROXEN SODIUM | 220 mg | |
| Product Characteristics | | Color | BLUE (Light Blue) | Score | no score | | Shape | ROUND | Size | 10mm | | Flavor | | Imprint Code | L490 | | Contains | | |
| Packaging | | # | Item Code | Package Description | | 1 | NDC:11673-490-78 | 1 BOTTLE (BOTTLE) in 1 CARTON | | 1 | | 100 TABLET (TABLET) in 1 BOTTLE | |
|
| Marketing Information | | Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date | | ANDA | ANDA074661 | 07/14/2009 | | |
| Labeler - Target Corporation (006961700) |
Revised: 05/2009 Target Corporation