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Pill Identifier Information of Ibuprofen 200 MG Oral Capsule

Drug Information

Ibuprofen 200 MG Oral Capsule

Imprint: 44;393
Shape: C48336
Color: C48331
Ingredients: Ibuprofen
Size: 14.00
Score: 1
Rxtty: SCD
Author: H E B
Inactive Ingredients: CARNAUBA WAX / FD&C YELLOW NO. 6 / HYPROMELLOSES / LACTOSE / MAGNESIUM STEARATE / POLYDEXTROSE / POLYETHYLENE GLYCOLS / SODIUM STARCH GLYCOLATE TYPE A POTATO / STEARIC ACID / TITANIUM DIOXIDE>

Complete Information

  • Active ingredient (in each orange 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
      • toothache
      • backache
      • menstrual cramps
      • the common cold
      • 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:

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

    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

    • 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

    Ask a doctor or pharmacist before use if you are

    When using this product

    Stop use and ask a doctor if
  • you have symptoms of heart problems or stroke:
  • 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

  • children under 12 years: ask a doctor
  • Other information

  • Inactive ingredients

    carnauba wax, colloidal silicon dioxide, corn starch, FD&C yellow #6 aluminum lake, hypromellose, lactose anhydrous, magnesium stearate, microcrystalline cellulose, polydextrose, polyethylene glycol, 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

    Compare to Motrin® IB
    Caplets     active ingredient†

    NDC 37808-393-12

    H-E-B®

    Ibuprofen
    Tablets USP, 200 mg
    Pain Reliever/Fever Reducer
    (NSAID)

    For Body Aches and Pains

    actual
    size

    100 COATED 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
    Johnson & Johnson Corporation, owner of the registered
    trademark Motrin® IB Caplets.

    50844    REV1221B39312

    MADE WITH PRIDE AND CARE FOR
    H-E-B®, SAN ANTONIO, TX 78204

    H-E-B®
    100%
    GUARANTEE
    promise

    If you aren't completely
    pleased with this product,
    we'll be happy to replace it
    or refund your money.
    You have our word on it.

    HEB 44-393

    HEB 44-393

  • INGREDIENTS AND APPEARANCE
    IBUPROFEN 
    ibuprofen tablet, film coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-393
    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)  
    FD&C YELLOW NO. 6 ALUMINUM LAKE (UNII: GYP6Z2JR6Q)  
    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
    ColororangeScoreno score
    ShapeOVALSize14mm
    FlavorImprint Code 44;393
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37808-393-121 in 1 CARTON03/01/1999
    1100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2NDC:37808-393-13250 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/01/1999
    3NDC:37808-393-20225 in 1 BOTTLE; Type 0: Not a Combination Product03/01/199910/25/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07513903/01/1999
    Labeler - H E B (007924756)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.038154464pack(37808-393)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.832867837manufacture(37808-393) , pack(37808-393)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.832867894manufacture(37808-393)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.868734088manufacture(37808-393)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.967626305pack(37808-393)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.117025878manufacture(37808-393)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.117597853pack(37808-393)