ALL DAY PAIN RELIEF- naproxen sodium tablet, film coated 
WALMART INC.

----------

Equate 44-604

Active ingredient (in each caplet)

Naproxen sodium 220 mg (naproxen 200 mg) (NSAID)*
*nonsteroidal anti-inflammatory drug

Purpose

Pain reliever/fever reducer

Uses

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

  • 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 have problems or serious side effects from taking pain relievers or fever reducers
  • you are taking a diuretic

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
    • leg swelling
    • chest pain
    • slurred speech
    • trouble breathing
    • weakness in one part or side of body
  • 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.

Directions

Other information

Inactive ingredients

croscarmellose sodium, FD&C blue #2 aluminum lake, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, povidone, silicon dioxide, talc, titanium dioxide

Questions or comments?

1-888-287-1915

Principal display panel

equate™

NDC 79903-005-10

Compare to Aleve® Caplets active ingredient**

All Day
Pain Relief

Naproxen Sodium
Tablets, 220 mg

Pain reliever/Fever reducer (NSAID)

12 HOURS

Actual Size

220
mg
EACH

40
CAPLETS†

†Capsule-Shaped Tablets

Satisfaction guaranteed – Or we'll replace it or
give you your money back. For questions or
comments or to report an undesired reaction
or side effect, please call 1-888-287-1915.

DISTRIBUTED BY: Walmart Inc.,
Bentonville, AR 72716

PRODUCT OF CHINA AND INDIA

**This product is not manufactured or
distributed by Bayer HealthCare LLC, owner
of the registered trademark Aleve® Caplets.

50844 REV1221A60410

Equate 44-604

Equate 44-604

ALL DAY PAIN RELIEF 
naproxen sodium tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-005
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
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
FD&C BLUE NO. 2--ALUMINUM LAKE (UNII: 4AQJ3LG584)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
TALC (UNII: 7SEV7J4R1U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColorblueScoreno score
ShapeOVALSize12mm
FlavorImprint Code 44;604
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79903-005-101 in 1 CARTON10/22/2020
140 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2NDC:79903-005-99100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/22/2020
3NDC:79903-005-751 in 1 CARTON10/22/2020
3100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
4NDC:79903-005-12100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/22/2020
5NDC:79903-005-30300 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/22/2020
6NDC:79903-005-25225 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/22/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20487210/22/2020
Labeler - WALMART INC. (051957769)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.038154464pack(79903-005)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867837manufacture(79903-005) , pack(79903-005)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867894manufacture(79903-005)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.967626305pack(79903-005)

Revised: 7/2023
Document Id: 43dbf861-15a0-4a1f-95a7-359586092784
Set id: c4909e43-57ba-44bc-a234-a02cc884891c
Version: 7
Effective Time: 20230706
 
WALMART INC.