PAIN RELIEF IBUPROFEN- ibuprofen tablet, film coated 
Rite Aid Corporation

----------

Rite Aid 44-292

Active ingredient (in each brown caplet)

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

  • 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

  • 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
  • stomach bleeding warning applies to you
  • 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 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

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 8:30 AM-4:00 PM ET, Monday-Friday

Principal Display Panel

NDC 11822-0292-4

Compare to the
active ingredient in
Advil® Caplets†

PAIN RELIEF
IBUPROFEN
IBUPROFEN TABLETS USP, 200 mg

PAIN RELIEVER/FEVER REDUCER
(NSAID)

ACTUAL SIZE

500
CAPLETS**
(**CAPSULE-SHAPED TABLETS)

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

†This product is not manufactured or distributed by PF
Consumer Healthcare 1 LLC, owner of the registered trademark
Advil® Caplets.       50844           REV1221A29214

DISTRIBUTED BY:
RITE AID, 200 NEWBERRY COMMONS
ETTERS, PA 17319 www.riteaid.com

SATISFACTION GUARANTEE:
If you’re not satisfied, we’ll
happily refund your money.

Rite Aid 44-292

Rite Aid 44-292

PAIN RELIEF IBUPROFEN 
ibuprofen tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-0292
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
Inactive Ingredients
Ingredient NameStrength
CARNAUBA WAX (UNII: R12CBM0EIZ)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
STARCH, CORN (UNII: O8232NY3SJ)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
POLYDEXTROSE (UNII: VH2XOU12IE)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColorbrownScoreno score
ShapeOVALSize14mm
FlavorImprint Code 44;292
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11822-0292-51 in 1 CARTON05/24/1988
150 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2NDC:11822-0292-21 in 1 CARTON05/24/1988
2100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3NDC:11822-0292-4500 in 1 BOTTLE; Type 0: Not a Combination Product05/24/1988
4NDC:11822-0292-81 in 1 BLISTER PACK05/24/198803/12/2023
42 in 1 BLISTER PACK; Type 0: Not a Combination Product
5NDC:11822-0292-61 in 1 CARTON05/24/198810/08/2021
516 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
6NDC:11822-0292-71 in 1 CARTON05/24/198810/08/2021
6125 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07501005/24/1988
Labeler - Rite Aid Corporation (014578892)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.038154464pack(11822-0292)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867837manufacture(11822-0292)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867894manufacture(11822-0292)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.967626305pack(11822-0292)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.117025878manufacture(11822-0292)

Revised: 2/2024
Document Id: c84ad8e1-1bdb-4215-86c5-ffb185360bc6
Set id: c85c3d1f-7639-4cfa-bf3a-424b61757b1a
Version: 23
Effective Time: 20240206
 
Rite Aid Corporation