IBUPROFEN- ibuprofen tablet, film coated 
REMEDYREPACK INC.

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OTC - ACTIVE INGREDIENT

Ibuprofen USP, 200 mg (NSAID)*

*nonsteroidal anti-inflammatory drug

 

OTC - PURPOSE

Pain reliever/fever reducer

 

INDICATIONS & USAGE

  • Temporarily relieves minor aches and pains due to:
    • headache
    • toothache
    • backache
    • menstrual cramps
    • the common cold
    • muscular aches
    • minor pain of arthritis
  • Temporarily reduces fever

 

WARNINGS

Allergy Alert: Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include:

  • shock
  • hives
  • facial swelling
  • asthma (wheezing)
  • 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 problems or serious side effects from taking pain relievers or fever reducers
  • you have a history of stomach problems, such as heartburn
  • you have high blood pressure, heart disease, liver cirrhosis, kidney disease or asthma
  • 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
    ibuprofen may decrease this benefit of aspirin
  • 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
  • redness or swelling is present in the painful area
  • fever gets worse or lasts more than 3 days
  • any new symptoms occur

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 right away.

 

DOSAGE & ADMINISTRATION

  • do not use more than directed
  • the smallest effective dose should be used
  • do not take longer than 10 days, unless directed by a doctor (see Warnings)
  • 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 take more than 6 tablets in 24 hours unless directed by a doctor
  • children under 12 years: ask a doctor

 

STORAGE AND HANDLING

  • store at controlled room temperature
  • avoid excessive heat 40°C (104°F)

 

INACTIVE INGREDIENT

carnauba wax, cellulose, corn starch, fumed silica gel, hypromellose, lactose, magnesium stearate, polydextrose, PEG, red iron oxide, sodium starch glycolate, stearic acid, titanium dioxide.

 

Call 1-800-540-3765

 

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION

DRUG: Ibuprofen


GENERIC: ibuprofen


DOSAGE: TABLET, FILM COATED


ADMINSTRATION: ORAL


NDC: 61786-181-33


ACTIVE INGREDIENT(S):

  • IBUPROFEN 200mg in 1


INACTIVE INGREDIENT(S):

  • CARNAUBA WAX
  • FERRIC OXIDE RED
  • POLYETHYLENE GLYCOLS
  • POLYDEXTROSE
  • SODIUM STARCH GLYCOLATE TYPE A POTATO
  • STEARIC ACID
  • CELLULOSE, MICROCRYSTALLINE
  • HYPROMELLOSES
  • SILICON DIOXIDE
  • STARCH, CORN
  • LACTOSE
  • MAGNESIUM STEARATE
  • TITANIUM DIOXIDE


COLOR: brown


SHAPE: ROUND


SCORE: No score


SIZE: 10 mm


IMPRINT: 44291


PACKAGING: 1000 in 1 BOTTLE




MM1

MM2

IBUPROFEN 
ibuprofen tablet, film coated
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:61786-181(NDC:57896-941)
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)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
POLYDEXTROSE (UNII: VH2XOU12IE)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
STARCH, CORN (UNII: O8232NY3SJ)  
LACTOSE (UNII: J2B2A4N98G)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColorbrownScoreno score
ShapeROUND (TABLET, FILM COATED) Size10mm
FlavorImprint Code 44291
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:61786-181-331000 in 1 BOTTLE; Type 0: Not a Combination Product02/11/201505/18/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07501002/11/201505/18/2016
Labeler - REMEDYREPACK INC. (829572556)

Revised: 3/2017
 
REMEDYREPACK INC.