Label: UP AND UP NAPROXEN SODIUM- naproxen sodium capsule, liquid filled 

  • Label RSS
  • NDC Code(s): 11673-742-06, 11673-742-27, 11673-742-58
  • Packager: Target Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Drug Application

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 02/13

If you are a consumer or patient please visit this version.

  • Active ingredient (in each capsule)

    Naproxen sodium 220 mg (naproxen 200 mg) (NSAID)*

    *nonsteroidal anti-inflammatory drug

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  • Purpose

    Pain reliever/fever reducer

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  • 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
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  • 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

    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, or kidney disease
    you are taking a diuretic
    you have problems or serious side effects from taking pain relievers or fever reducers
    you have asthma

    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
    the risk of heart attack or stroke may increase if you use more than directed or for longer than directed

    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
    pain gets worse or lasts more than 10 days
    fever gets worse or lasts more than 3 days
    redness or swelling is present in the painful area
    any new symptoms appear
    you have difficulty swallowing
    it feels like the capsule is stuck in your throat

    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)

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  • Directions

    do not take more than directed
    the smallest effective dose should be used
    drink a full glass of water with each dose
    if taken with food, this product may take longer to work

    adults and children 12 years and older:

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

    children under 12 years:

    ask a doctor
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  • Other information

    each capsule contains: sodium 20 mg
    store at 20-25°C (68-77°F) avoid high humidity and excessive heat above 40°C (104°F)
    do not use if printed foil under cap is broken or missing
    read all directions and warnings before use. Keep carton.
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  • Inactive ingredients

    FD&C blue #1, gelatin, glycerin, lactic acid, mannitol, pharmaceutical ink, polyethylene glycol, povidone, propylene glycol, purified water, sorbitan, sorbitol

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  • Questions?

    Call 1-800-910-6874

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  • Package/Label Principal Display Panel

    naproxen sodium capsules, 220 mg (NSAID)

    pain reliever/fever reducer

    Compare to the active ingredient of Aleve® Liquid Gels

    strength to last 12 hours

    ACTUAL SIZE

    # LIQUID GELS** {Replace "#" with the number of liquidgels in the product}

    (**LIQUID-FILLED CAPSULES)

    Naproxen Sodium Capsules, 220 mg (NSAID) Carton Image
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  • INGREDIENTS AND APPEARANCE
    UP AND UP NAPROXEN SODIUM 
    naproxen sodium capsule, liquid filled
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:11673-742
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    NAPROXEN SODIUM (NAPROXEN) NAPROXEN SODIUM 220 mg
    Inactive Ingredients
    Ingredient Name Strength
    FD&C BLUE NO. 1  
    GELATIN  
    GLYCERIN  
    LACTIC ACID  
    MANNITOL  
    POLYETHYLENE GLYCOLS  
    POVIDONES  
    PROPYLENE GLYCOL  
    WATER  
    SORBITAN  
    SORBITOL  
    Product Characteristics
    Color BLUE (Clear) Score no score
    Shape CAPSULE Size 20mm
    Flavor Imprint Code 742
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:11673-742-27 1 in 1 CARTON
    1 80 in 1 BOTTLE
    2 NDC:11673-742-06 1 in 1 CARTON
    2 160 in 1 BOTTLE
    3 NDC:11673-742-58 1 in 1 CARTON
    3 40 in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    NDA NDA021920 01/05/2011
    Labeler - Target Corporation (006961700)
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