Label: NAPROXEN SODIUM tablet

  • NDC Code(s): 69848-009-01, 69848-010-01, 69848-010-05, 69848-010-10
  • Packager: Granules USA, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated January 2, 2024

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

  • Active ingredient (For Tablet)

    (in each tablet)

    Naproxen sodium 220 mg

    (naproxen 200 mg) (NSAID)**

    **nonsteroidal anti-inflammatory drug

  • Active ingredient (For Caplet)

    (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

  • 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 the reach of children.

    In case of overdose, get medical help or contact a Poison Control Center right away.

  • Directions (For Tablets)

    ■ 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 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

    ■ ask a doctor

  • Directions (For Caplets)

    ■ 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 (For Tablet)

    ■ each tablet contains: sodium 20 mg

    ■ store at 20 - 25°C (68 - 77°F). Avoid high humidity and excessive heat above 40°C (104°F)

  • Other information (For Caplet)

    each caplet contains: sodium 20 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 #2 aluminum lake, hypromellose 2910, maize starch, microcrystalline cellulose, polyethylene glycol, povidone k-30, sodium starch glycolate, stearic acid, titanium dioxide.

  • Questions or comments?

    1-877-770-3183 Mon - Fri 9:00 AM to 4:00 PM EST.

  • Tablets

    10 count

  • Caplets

    100ct carton50ct carton10 count

  • INGREDIENTS AND APPEARANCE
    NAPROXEN SODIUM 
    naproxen sodium tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69848-010
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NAPROXEN SODIUM (UNII: 9TN87S3A3C) (NAPROXEN - UNII:57Y76R9ATQ) NAPROXEN SODIUM220 mg
    Inactive Ingredients
    Ingredient NameStrength
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    FD&C BLUE NO. 2 (UNII: L06K8R7DQK)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    POVIDONE (UNII: FZ989GH94E)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    Product Characteristics
    ColorblueScoreno score
    ShapeROUNDSize10mm
    FlavorImprint Code 220
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69848-010-0110 in 1 BOTTLE; Type 0: Not a Combination Product07/01/2019
    2NDC:69848-010-0550 in 1 BOTTLE; Type 0: Not a Combination Product03/01/2023
    3NDC:69848-010-10100 in 1 BOTTLE; Type 0: Not a Combination Product03/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA09135307/01/2019
    NAPROXEN SODIUM 
    naproxen sodium tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69848-009
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NAPROXEN SODIUM (UNII: 9TN87S3A3C) (NAPROXEN - UNII:57Y76R9ATQ) NAPROXEN SODIUM220 mg
    Inactive Ingredients
    Ingredient NameStrength
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    POVIDONE (UNII: FZ989GH94E)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    FD&C BLUE NO. 2 (UNII: L06K8R7DQK)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    Product Characteristics
    ColorblueScoreno score
    ShapeOVALSize12mm
    FlavorImprint Code 220
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69848-009-0110 in 1 BOTTLE; Type 0: Not a Combination Product07/01/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA09135307/01/201912/31/2023
    Labeler - Granules USA, Inc. (137098864)