Active Ingredient
(in each tablet)
Naproxen sodium 220 mg (NSAID)**
**nonsteroidal anti-inflammatory drug
The following Structured Product Label (SPL) was submitted to the FDA by Pharmacy Valuce Alliance, Llc for the product Naproxen Sodium (NDC 68016-661). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purposes, uses, allergy alert, stomach bleeding warning, heart attack and stroke warning:, do not use, ask a doctor before use if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
(in each tablet)
Naproxen sodium 220 mg (NSAID)**
**nonsteroidal anti-inflammatory drug
Pain reliever/fever reducer
■ minor pain of arthritis
■ muscular aches
■ backache
■ menstrual cramps
■ headache
■ toothache
■ the common cold
Naproxen sodium may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include:
If an allergic reaction occurs, stop use and seek medical help right away.
This product contains an NSAID, which may cause severe stomach bleeding.
The chance is higher if you:
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.
■ feel faint
■ vomit blood
■ have bloody or black stools
■ have stomach pain that does not get better
■ chest pain
■ trouble breathing
■ weakness in one part or side of body
■ slurred speech
■ leg swelling
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.
In case of overdose, get medical help or contact a Poison Control Center right away
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
FD&C blue #2 aluminum lake, hypromellose 2910, maize starch, microcrystalline cellulose, polyethylene glycol, povidone k-30, sodium starch glycolate, stearic acid, titanium dioxide.
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* Please review the disclaimer below.