NAPROXEN SODIUM- naproxen sodium tablet 
Pharmacy Valuce Alliance, LLC

----------

Naproxen Sodium Tablets USP 220mg (Round)

Active ingredient

(in each tablet)

Naproxen sodium 220 mg (NSAID)**

**nonsteroidal anti-inflammatory drug

Purposes

Pain reliever/fever reducer

Uses

■ minor pain of arthritis

■ muscular aches

■ backache

■ menstrual cramps

■ headache

■ toothache

■ the common cold

Warnings

Allergy alert

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.

Stomach bleeding warning

This product contains an NSAID, which may cause severe stomach bleeding.

The chance is higher if you:

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

Ask a doctor before use if

Ask a doctor or pharmacist before use if you are

When using this product

Stop use and ask a doctor if

■ 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

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

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

Other information

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.

100 count

50 count

NAPROXEN SODIUM 
naproxen sodium tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-661
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)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
STARCH, CORN (UNII: O8232NY3SJ)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
POVIDONE K30 (UNII: U725QWY32X)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
FD&C BLUE NO. 2 (UNII: L06K8R7DQK)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
Product Characteristics
ColorblueScoreno score
ShapeROUNDSize10mm
FlavorImprint Code 220
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68016-661-10100 in 1 BOTTLE; Type 0: Not a Combination Product02/25/2016
2NDC:68016-661-0550 in 1 BOTTLE; Type 0: Not a Combination Product02/25/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA09135302/25/2016
Labeler - Pharmacy Valuce Alliance, LLC (101668460)

Revised: 1/2021
Document Id: ba16adf1-6f4f-b473-e053-2a95a90a7219
Set id: 3da8843c-e8bb-164d-e054-00144ff8d46c
Version: 4
Effective Time: 20210129
 
Pharmacy Valuce Alliance, LLC