NAPROXEN SODIUM - naproxen sodium tablet, film coated 
Camber Consumer Care Inc

----------

Naproxen Sodium Tablets USP, 220 mg (NSAID)

ACTIVE INGREDIENT(S)

(in each tablet)
Naproxen sodium USP 220 mg (naproxen 200 mg) (NSAID)*                                                          
*nonsteroidal anti-inflammatory drug

PURPOSE

Pain reliever/ fever reducer
               


USE(S)


• temporarily relieves minor aches and pains due to:
   • minor pain of arthritis
   • muscular aches
   • backache
   • headache
   • the common cold
   • menstrual cramps 
   • toothache
• 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, 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 aspirin for heart attack or stroke, because naproxen may decrease this benefit of aspirin
• 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

PREGNANCY/BREASTFEEDING


If pregnant or breast-feeding, ask a health professional before use. It is especially important not to use naproxen sodium at 20 weeks or later in 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.

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 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


 each tablet 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


corn starch, FD&C blue #2, hypromellose, microcrystalline cellulose, polyethylene glycol, povidone, sodium starch glycolate, stearic acid, talc and titanium dioxide.

QUESTIONS OR COMMENTS?

1-888-588-1418 (Mon - Fri 9AM - 5PM EST)
 
Do not use if bottle is open or if foil seal imprinted with "SEALED for YOUR PROTECTION" on bottle opening is missing or broken.
 

Mfg. Lic. No.: 24/MD/TS/2016/F/G


Distributed by:
Camber Consumer Care, Inc.
Piscataway, NJ 08854, USA.

PRINCIPAL DISPLAY PANEL


Naproxen Sodium Round Shape 100's container Label

naproxensodium-round-100s-cont-label


 
Naproxen Sodium Round Shape 100's container Carton Label



naproxensodium-round-100s-cont-carton-label

NAPROXEN SODIUM  
naproxen sodium tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69230-329
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
STARCH, CORN (UNII: O8232NY3SJ)  
FD&C BLUE NO. 2 (UNII: L06K8R7DQK)  
HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)  
MICROCRYSTALLINE CELLULOSE 101 (UNII: 7T9FYH5QMK)  
POVIDONE K30 (UNII: U725QWY32X)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TALC (UNII: 7SEV7J4R1U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
Product Characteristics
ColorblueScoreno score
ShapeROUNDSize10mm
FlavorImprint Code H;N11
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69230-329-241 in 1 CARTON10/28/2022
124 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:69230-329-501 in 1 CARTON10/28/2022
250 in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:69230-329-011 in 1 CARTON10/28/2022
3100 in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:69230-329-021 in 1 CARTON10/28/2022
4200 in 1 BOTTLE; Type 0: Not a Combination Product
5NDC:69230-329-05500 in 1 BOTTLE; Type 0: Not a Combination Product10/28/2022
6NDC:69230-329-101000 in 1 BOTTLE; Type 0: Not a Combination Product10/28/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21106510/28/2022
Labeler - Camber Consumer Care Inc (079539968)
Establishment
NameAddressID/FEIBusiness Operations
Annora Pharma Private Limited650980746manufacture(69230-329)

Revised: 11/2022
Document Id: ee21e0f7-9f32-6c63-e053-2a95a90ac996
Set id: d1008e19-ff0d-4ed2-909d-bae5a82a1234
Version: 1
Effective Time: 20221123
 
Camber Consumer Care Inc