NAPROXEN SODIUM CAPLETS- naproxen sodium tablet 
Yichang Humanwell Pharmaceutical Co., Ltd.

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Naproxen Sodium Tablets USP, 220 mg

Drug Facts

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, or 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

  • side effects occur. You may report side effects to FDA at 1-800-FDA-1088.
  • you experience any of the following signs of stomach bleeding:

    o feel faint

    o vomit blood

    o have bloody or black stools

    o have stomach pain that does not get better

  • you have symptoms of heart problems or stroke:

    o chest pain
    o trouble breathing
    o weakness in one part or side of body
    o slurred speech
    o 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

Croscarmellose sodium, FD&C blue #1, FD&C blue #2, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, povidone, talc and titanium dioxide.

Questions or comments?

1-650-289-8840 (Mon-Fri 9AM-5PM EST)

You may also report side effects to this phone number.

PRINCIPAL DISPLAY PANEL - 24 and 100 Caplet Bottle Carton

NDC 62732-1026-1

Naproxen Sodium Tablets USP, 220 mg (NSAID)

Pain Reliever/Fever Reducer

STRENGTH TO LAST 12 HOURS

24 CAPLETS

CAPSULE-SHAPED TABLETS

220mg-24ct

NDC 62732-1026-2

Naproxen Sodium Tablets USP, 220 mg (NSAID)

Pain Reliever/Fever Reducer

STRENGTH TO LAST 12 HOURS

100 CAPLETS

CAPSULE-SHAPED TABLETS

220mg-100ct

NAPROXEN SODIUM  CAPLETS
naproxen sodium tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62732-1026
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
POVIDONE K30 (UNII: U725QWY32X)  
MICROCRYSTALLINE CELLULOSE 102 (UNII: PNR0YF693Y)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
TALC (UNII: 7SEV7J4R1U)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)  
FD&C BLUE NO. 2 (UNII: L06K8R7DQK)  
Product Characteristics
Colorblue (Light blue) Scoreno score
ShapeOVAL (caplets shaped tablets) Size12mm
FlavorImprint Code YH172
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62732-1026-11 in 1 CARTON12/31/202004/20/2021
124 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:62732-1026-21 in 1 CARTON12/31/202004/20/2021
2100 in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:62732-1026-31000 in 1 BOTTLE; Type 0: Not a Combination Product12/31/202004/20/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21203312/31/202004/20/2021
Labeler - Yichang Humanwell Pharmaceutical Co., Ltd. (527225336)
Establishment
NameAddressID/FEIBusiness Operations
Yichang Humanwell Oral Solid Dosage Plant421371958manufacture(62732-1026)

Revised: 4/2021
 
Yichang Humanwell Pharmaceutical Co., Ltd.