Label: PAIN RELIEF IBUPROFEN- ibuprofen tablet, film coated
- NDC Code(s): 11822-0392-2, 11822-0392-4, 11822-0392-5
- Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated October 9, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each orange tablet)
- Purpose
- Uses
-
Warnings
Allergy alert: Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include:
- skin reddening
- asthma (wheezing)
- rash
- facial swelling
- shock
- blisters
- hives
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
- take more or for a longer time than directed
- take a blood thinning (anticoagulant) or steroid drug
- are age 60 or older
- take other drugs containing prescription or nonprescription NSAIDs [aspirin, ibuprofen, naproxen, or others]
- have had stomach ulcers or bleeding problems
- have 3 or more alcoholic drinks every day while using this product
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
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
- slurred speech
- leg swelling
- 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
- redness or swelling is present in the painful area
- any new symptoms appear
- skin reddening
-
Directions
-
do not take more than directed
- the smallest effective dose should be used
- adults and children 12 years and over: take 1 tablet every 4 to 6 hours while symptoms persist
- if pain or fever does not respond to 1 tablet, 2 tablets may be used
- do not exceed 6 tablets in 24 hours, unless directed by a doctor
- children under 12 years: ask a doctor
-
do not take more than directed
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal Display Panel
Compare to the active
ingredient in Motrin® IB Tablets**NDC 11822-0392-4
PAIN RELIEF
IBUPROFEN
IBUPROFEN TABLETS USP, 200 mgPAIN RELIEVER
FEVER REDUCER
(NSAID)ACTUAL SIZE
500
TABLETSTAMPER EVIDENT: DO NOT USE IF IMPRINTED
SAFETY SEAL UNDER CAP IS BROKEN OR MISSING
**This product is not manufactured or distributed
by Johnson & Johnson Corporation, owner of the
registered trademark Motrin® IB Tablets.
50844 ORG122139214DISTRIBUTED BY:
RITE AID
30 HUNTER LANE
CAMP HILL, PA 17011
www.riteaid.comSATISFACTION GUARANTEE:
If you’re not satisfied, we’ll
happily refund your money.
Rite Aid 44-392
-
INGREDIENTS AND APPEARANCE
PAIN RELIEF IBUPROFEN
ibuprofen tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-0392 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 CARNAUBA WAX (UNII: R12CBM0EIZ) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) STARCH, CORN (UNII: O8232NY3SJ) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYDEXTROSE (UNII: VH2XOU12IE) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2) STEARIC ACID (UNII: 4ELV7Z65AP) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color orange Score no score Shape ROUND Size 10mm Flavor Imprint Code 44;392 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-0392-2 1 in 1 CARTON 03/30/2002 1 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:11822-0392-4 500 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/30/2002 3 NDC:11822-0392-5 1 in 1 CARTON 03/30/2002 03/05/2022 3 50 in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA075139 03/30/2002 Labeler - Rite Aid Corporation (014578892) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(11822-0392) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(11822-0392) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(11822-0392) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 manufacture(11822-0392) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(11822-0392) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(11822-0392)