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Flanax Pain Reliever

Dosage form: tablet
Ingredients: Naproxen Sodium 220mg
Labeler: Belmora LLC
NDC Code: 27854-103

Flanax® Pain Reliever

Drug Facts

Active Ingredient (in each tablet)

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

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 reliever 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
  • 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.

  • 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 24-hour period
Children under 12 years
  • ask a doctor

Other Information
  • 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)

Inactive ingredients

Croscarmellose sodium, FD&C Blue #2, macrogol, magnesium stearate, polyvinyl alcohol, povidone, pregelatinized starch, talc and titanium dioxide

Questions or Comments

Call 1-888-535-2629 M-F, 9AM-5PM CST
www.flanaxusa.com

Distributed by Belmora
LLC, PO Box 3063 Arlington, VA 22203

PRINCIPAL DISPLAY PANEL - 24 Tablet Bottle Carton

Belmora LLC

FLANAX®

PAIN RELIEVER/FEVER REDUCER

24
220MG TABLETS NAPROXEN SODIUM USP (NSAID)

FLANAX PAIN RELIEVER 
naproxen sodium tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:27854-103
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Naproxen Sodium (Naproxen) Naproxen Sodium220 mg
Inactive Ingredients
Ingredient NameStrength
HYPROMELLOSES 
FD&C BLUE NO. 2 
MAGNESIUM STEARATE 
POLYETHYLENE GLYCOLS 
POVIDONES 
TALC 
TITANIUM DIOXIDE 
CELLULOSE, MICROCRYSTALLINE 
POLYSORBATE 80 
Product Characteristics
ColorBLUEScore2 pieces
ShapeROUNDSize10mm
FlavorHONEYImprint CodeI3
Contains    
Packaging
#Item CodePackage Description
1NDC:27854-103-0124 TABLET in 1 BOTTLE
2NDC:27854-103-0410 TABLET in 1 BOTTLE
3NDC:27854-103-061 TABLET in 1 POUCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07909612/06/2012
Labeler - Belmora LLC (112753244)
Registrant - Amneal Pharmaceutical (123797875)
Establishment
NameAddressID/FEIOperations
Belmora LLC112753244LABEL(27854-103)
Establishment
NameAddressID/FEIOperations
Amneal Pharmaceutical968119730MANUFACTURE(27854-103)

Revised: 12/2012
 
Belmora LLC

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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