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All Day Pain Relief by We Care Distributor Inc.

Medically reviewed on February 12, 2018

Dosage form: tablet
Ingredients: NAPROXEN SODIUM 220mg
Labeler: We Care Distributor Inc.
NDC Code: 70005-008

All Day Pain Relief - Naproxen Sodium Tablets, 220 mg

Drug Facts

Active ingredients (in each tablet)Purposes
*
Naproxen Sodium 220 mg 
(naproxen 200 mg) (NSAID)Pain reliever/fever reducer

*nonsteroidal anti-inflammatory drug

Uses

■ temporarily relieves minor aches and pains due to:

  ■ minor pain of arthritis ■ muscular aches ■ backache ■ headache

  ■ menstrual cramps ■ 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 relievers or fever reducers

■ you have asthma

■ 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 (1-800-222-1222) right away. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

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

  ■ take 1 tablet every 8 to 12 hours while symptoms last 12 years and older

  ■ 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 20 mg

■ store at 20-25°C (68-77°F). Avoid high humidity and excessive heat above 40°C (104°F)

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?

1-888-705-WECARE (Mon-Fri 9am-5pm EST) or www.wecaredistributor.com

PRINCIPAL DISPLAY PANEL

See New Warnings Information & Directions

Compare to the Active Ingredients in Aleve®.

ALL DAY PAIN RELIEF

Naproxen Sodium Tablets, 220 mg

TO OPEN
PUSH IN TAB AND PULL OUT

25 Pouches of 2 Caplets Each

ALL DAY PAIN RELIEF 
naproxen sodium tablets, 220 mg tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70005-008
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NAPROXEN SODIUM (NAPROXEN) NAPROXEN220 mg
Inactive Ingredients
Ingredient NameStrength
HYPROMELLOSES 
FD&C BLUE NO. 2 
POVIDONE K30 
STARCH, CORN 
SODIUM STARCH GLYCOLATE TYPE A POTATO 
CELLULOSE, MICROCRYSTALLINE 
POLYETHYLENE GLYCOL 400 
STEARIC ACID 
TITANIUM DIOXIDE 
Product Characteristics
ColorBLUE (Light Blue) Scoreno score
ShapeOVAL (Capsule-Shaped) Size12mm
FlavorImprint Code220
Contains    
Packaging
#Item CodePackage Description
1NDC:70005-008-2525 POUCH in 1 BOX
12 TABLET in 1 POUCH
2NDC:70005-008-5050 POUCH in 1 BOX
22 TABLET in 1 POUCH
3NDC:70005-008-022 POUCH in 1 POUCH
32 TABLET in 1 POUCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA09135309/30/2011
Labeler - We Care Distributor Inc. (079832998)
Establishment
NameAddressID/FEIOperations
Elysium Pharmaceutical Ltd.915664486manufacture(70005-008)

 
We Care Distributor Inc.

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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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