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up and up naproxen sodium (Target Corporation)

Available Formats

Dosage Form Package Information Links
TABLET, FILM COATED 1 BOTTLE in 1 CARTON (11673-368-78) > 100 TABLET, FILM COATED in 1 BOTTLE Label Information
TABLET, FILM COATED 1 BOTTLE in 1 CARTON (11673-368-71) > 50 TABLET, FILM COATED in 1 BOTTLE Label Information
TABLET, FILM COATED 1 BOTTLE in 1 CARTON (11673-368-82) > 200 TABLET, FILM COATED in 1 BOTTLE Label Information
TABLET, FILM COATED 300 TABLET, FILM COATED in 1 BOTTLE (11673-368-87) Label Information
TABLET, FILM COATED 1 BOTTLE in 1 CARTON (11673-368-76) > 120 TABLET, FILM COATED in 1 BOTTLE Label Information

Complete up and up naproxen sodium Information

  • Active ingredient (in each caplet)

    Naproxen sodium 220 mg

    (naproxen 200 mg) (NSAID)*

    *nonsteroidal anti-inflammatory drug


  • Purposes

    Pain reliever/fever reducer


  • Uses

    • temporarily relieves minor aches and pains due to:
    • minor pain of arthritis
    • muscular aches
    • backache
    • menstrual cramps
    • headache
    • toothache
    • the common cold
    • temporarily reduces fever

  • Warnings

    Allergy alert: Naproxen sodium may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include:

    • hives
    • facial swelling
    • asthma (wheezing)
    • shock
    • skin reddening
    • rash
    • blisters

    If an allergic reaction occurs, stop use and seek medical help right away.

    Stomach bleeding warning: This product contains an NSAID, which may cause severe stomach bleeding. The chance is higher if you

    • are age 60 or older
    • have had stomach ulcers or bleeding problems
    • take a blood thinning (anticoagulant) or steroid drug
    • take other drugs containing prescription or nonprescription NSAIDs (aspirin, ibuprofen, naproxen, or others)
    • have 3 or more alcoholic drinks every day while using this product
    • take more or for a longer time than directed

    Heart attack and stroke warning: NSAIDs, except aspirin, increase the risk of heart attack, heart failure, and stroke. These can be fatal. The risk is higher if you use more than directed or for longer than directed.

    Do not use
    • if you have ever had an allergic reaction to any other pain reliever/fever reducer
    • right before or after heart surgery

    Ask a doctor before use if
    • the stomach bleeding warning applies to you
    • you have a history of stomach problems, such as heartburn
    • you have high blood pressure, heart disease, liver cirrhosis, kidney disease, asthma, or had a stroke
    • you are taking a diuretic
    • you have problems or serious side effects from taking pain relievers or fever reducers

    Ask a doctor or pharmacist before use if you are
    • under a doctor’s care for any serious condition
    • taking any other drug

    When using this product
    • take with food or milk if stomach upset occurs

    Stop use and ask a doctor if
    • you experience any of the following signs of stomach bleeding:
    • feel faint
    • vomit blood
    • have bloody or black stools
    • have stomach pain that does not get better
    • you have symptoms of heart problems or stroke:
    • chest pain
    • trouble breathing
    • weakness in one part or side of body
    • slurred speech
    • leg swelling
    • pain gets worse or lasts more than 10 days
    • fever gets worse or lasts more than 3 days
    • you have difficulty swallowing
    • it feels like the pill is stuck in your throat
    • redness or swelling is present in the painful area
    • any new symptoms appear

    If pregnant or breast-feeding,

    ask a health professional before use. It is especially important not to use naproxen sodium during the last 3 months of pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.

    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
    • the smallest effective dose should be used
    • drink a full glass of water with each dose

    Adults and

    children 12

    years and

    older

    • take 1 caplet every 8 to 12 hours while symptoms last
    • for the first dose you may take 2 caplets within the first hour
    • do not exceed 2 caplets in any 8- to 12-hour period
    • do not exceed 3 caplets in a 24-hour period

    Children

    under 12

    years

    • ask a doctor


  • Other information

    • each caplet contains: sodium 21 mg
    • store at 20-25°C (68-77°F). Avoid high humidity and excessive heat above 40°C (104°F).

  • Inactive ingredients

    FD&C blue no. 2 aluminum lake, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, povidone, talc, titanium dioxide


  • Questions or comments?

    1-888-547-7400


  • Principal Display Panel

    see new warnings

    Compare to active ingredient in Aleve® Caplets

    naproxen sodium tablets, 220 mg

    pain reliever/fever reducer (NSAID)

    strength to last 12 hours

    ACTUAL SIZE

    100 CAPLETS†

    100 CAPLETS† (†CAPSULE-SHAPED TABLETS)

    368-uw-naproxen-sodium.jpg

  • INGREDIENTS AND APPEARANCE
    UP AND UP NAPROXEN SODIUM 
    naproxen sodium tablet, film coated
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-368
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    NAPROXEN SODIUM (UNII: 9TN87S3A3C) (NAPROXEN - UNII:57Y76R9ATQ) NAPROXEN SODIUM 220 mg
    Inactive Ingredients
    Ingredient Name Strength
    FD&C BLUE NO. 2 (UNII: L06K8R7DQK)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
    POVIDONES (UNII: FZ989GH94E)  
    TALC (UNII: 7SEV7J4R1U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    Color BLUE (Light Blue) Score no score
    Shape OVAL Size 12mm
    Flavor Imprint Code L368
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:11673-368-71 1 in 1 CARTON 07/14/2009
    1 50 in 1 BOTTLE; Type 0: Not a Combination Product
    2 NDC:11673-368-78 1 in 1 CARTON 06/24/2009
    2 100 in 1 BOTTLE; Type 0: Not a Combination Product
    3 NDC:11673-368-82 1 in 1 CARTON 06/24/2009
    3 200 in 1 BOTTLE; Type 0: Not a Combination Product
    4 NDC:11673-368-87 300 in 1 BOTTLE; Type 0: Not a Combination Product 03/11/2010
    5 NDC:11673-368-76 1 in 1 CARTON 11/17/2011
    5 120 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    ANDA ANDA074661 06/24/2009
    Labeler - Target Corporation (006961700)