IBUPROFEN- ibuprofen tablet, film coated 
CVS Pharmacy

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CVS 44-291

Active ingredient (in each brown tablet)

Ibuprofen USP, 200 mg (NSAID)*
*nonsteroidal anti-inflammatory drug

Purpose

Pain reliever/fever reducer

Uses

Warnings

Allergy alert: Ibuprofen 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

  • right before or after heart surgery
  • if you have ever had an allergic reaction to any other pain reliever/fever reducer 

Ask a doctor before use if

  • stomach bleeding warning applies to you
  • you have a history of stomach problems, such as heartburn
  • you are taking a diuretic
  • 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

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 ibuprofen 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
  • leg swelling
  • slurred speech
  • 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
  • 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 ibuprofen 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.

Directions

Other information

Inactive ingredients

carnauba wax, colloidal silicon dioxide, corn starch, hypromellose, lactose anhydrous, magnesium stearate, microcrystalline cellulose, polydextrose, polyethylene glycol, red iron oxide, sodium starch glycolate, stearic acid, titanium dioxide

Questions or comments?

Call 1-800-426-9391 8:30AM-4:00PM ET, Monday-Friday

Principal Display Panel

♥︎CVS Health™

Compare to the active
ingredient in Advil® Tablets

Coated Tablets

NDC 59779-291-15

Ibuprofen
IBUPROFEN TABLETS USP, 200 mg

Pain reliever,
Fever reducer (NSAID)

50 COATED TABLETS

Actual Size

TAMPER EVIDENT: DO NOT USE IF IMPRINTED
SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

This product is not manufactured or distributed by Wyeth Consumer
Healthcare, owner of the registered trademark Advil® Tablets.
50844           REV1116A29115

Distributed by: CVS Pharmacy, Inc.
One CVS Drive, Woonsocket, RI 02895
© 2017 CVS/pharmacy    CVS.com®
1-800-SHOP CVS    V-11112


CVS 44-291

CVS 44-291

IBUPROFEN 
ibuprofen tablet, film coated
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-291
Route of Administration ORAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN 200 mg
Inactive Ingredients
Ingredient Name Strength
HYPROMELLOSES (UNII: 3NXW29V3WO)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
POLYDEXTROSE (UNII: VH2XOU12IE)  
POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
Color BROWN Score no score
Shape ROUND Size 10mm
Flavor Imprint Code 44;291
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:59779-291-98 2 in 1 PACKAGE 05/24/1988
1 10 in 1 BOTTLE; Type 0: Not a Combination Product
2 NDC:59779-291-96 2 in 1 PACKAGE 05/24/1988
2 400 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3 NDC:59779-291-15 1 in 1 CARTON 05/24/1988
3 50 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
4 NDC:59779-291-29 1 in 1 CARTON 05/24/1988
4 150 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
5 NDC:59779-291-12 1 in 1 CARTON 05/24/1988
5 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
6 NDC:59779-291-03 10 in 1 VIAL; Type 0: Not a Combination Product 05/24/1988
7 NDC:59779-291-05 400 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/24/1988
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA075010 05/24/1988
Labeler - CVS Pharmacy (062312574)
Establishment
Name Address ID/FEI Business Operations
LNK International, Inc. 832867894 MANUFACTURE(59779-291)
Establishment
Name Address ID/FEI Business Operations
LNK International, Inc. 038154464 PACK(59779-291)
Establishment
Name Address ID/FEI Business Operations
LNK International, Inc. 868734088 PACK(59779-291)
Establishment
Name Address ID/FEI Business Operations
LNK International, Inc. 832867837 PACK(59779-291)
Establishment
Name Address ID/FEI Business Operations
LNK International, Inc. 967626305 PACK(59779-291)

Revised: 7/2017
Document Id: de335c0f-b6d4-4327-ae34-63ae30010b2a
Set id: 8d9f11a5-ca98-4280-9c6a-093d32e60ace
Version: 12
Effective Time: 20170724
 
CVS Pharmacy