IBUPROFEN TABLET [GEISS, DESTIN & DUNN, INC (GOODSENSE)]

IBUPROFEN TABLET [GEISS, DESTIN & DUNN, INC (GOODSENSE)]
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NDC 50804-167-50
Set ID 71ec6245-dd01-4791-b6c8-1e0b849a2164
Category HUMAN OTC DRUG LABEL
Packager Good Sense (Geiss, Destin & Dunn, Inc.)
Generic Name
Product Class
Product Number
Application Number ANDA079174
  • Active Ingredient (in each caplet)

    Ibuprofen USP, 200 mg (NSAID)*

    *nonsteroidal anti-inflammatory drug

    Purpose

    Pain Reliever/ Fever Reducer

  • Uses

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

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

    • hives
    • facial swelling
    • asthma (wheezing)
    • shock
    • skin reddening
    • rash
    • blisters

    If an allergic reaction occurs, stop use an 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 oder
    • have had stomach ulders or bleeding problems
    • take blood thinning (anticoagulant) or steroid drug
    • take other drugs containing prescritpion or non-prescription NSAIDs (aspirin, ibuprofen, naproxen, or others)
    • have 3 or more alcoholic drinks everyday while using this prdouct
    • take more or for a longer time than directed.

    Do not use

    • if you 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 problems or serious side effects from taking pain relievers or fever reducers
    • 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, or kidney disease
    • you have asthma
    • you are taking a diuretic.

    Ask a doctor or pharmacist before use if you are

    • taking aspirin for heart attack or stroke, because ibuprofen may decrease this benefit of aspirin
    • under a doctor's care for any serious condition
    • 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 last more than 10 days
      • Fever gets worse or last 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 druing the last 3 months of pegnancy unless defintely 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 (1-800-222-1222)

    Directions

    • do not take more than directed
    • the smallest effective dose should be used
     Adults and children 12 years and older
    •  take 1 caplet every 4 to 6 hours while symptoms persist
    • if pain or fever does not respond to 1 caplet, 2 caplets may be used
    • do not exceed 6 caplets in 24 hours, unless directed by a doctor
     children under 12 years
    •  ask a doctor

    Other information

    • store between 20o- 25o C (68o- 77o F)
  • Inactive Ingredients

    colloidal silicon dioxide, corn starch, dextrose monohydrate, hypromellose, iron oxide red, lactose monohydrate, lecithin, maltodextrin, povidone (K-30), pregelatinized starch, sodium carboxymethylcellulose, sodium starch glycolate, stearic acid, titanium dioxide, and triacetin

  • Questions or comments?

    Call 1-877-753-3935 Monday through Friday 9AM-5PM EST

  • Principal Display Panel

    †Compare to the active ingredient in ADVIL® Ibuprofen caplets

    do not use if imprinted foil under cap is broken or missing

    READ ALL WARNINGS AND DIRECTIONS BEFORE USE. KEEP CARTON.

    †This product is not manufactured or distributed by Pfizer consumer healthcare, owner of the registered trademark Advil®

    Ibuprofen Tablets USP, 200 mg

    Pain Reliever/ Fever Reducer (NSAID)*

    Manufactured by:

    Granules India Limited

    Madhapur, Hyderabad- 500 081, India.

    KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION

  • Product Label

    Goodsense Ibuprofen caplets 200 mg

    Ibuprofen caplets 200 mg

  • INGREDIENTS AND APPEARANCE
    IBUPROFEN 
    ibuprofen tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50804-167
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
    Inactive Ingredients
    Ingredient NameStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    POVIDONE (UNII: FZ989GH94E)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    TRIACETIN (UNII: XHX3C3X673)  
    Product Characteristics
    ColorBROWN (reddish) Scoreno score
    ShapeCAPSULESize10mm
    FlavorImprint Code G2
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50804-167-501 in 1 BOX12/22/201112/30/2021
    150 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07917412/22/201112/30/2021
    Labeler - Good Sense (Geiss, Destin & Dunn, Inc.) (076059836)

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