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Panadol® Advance
2016-04-09 10:12:16 来源: 作者: 【 】 浏览:603次 评论:0
  • Active ingredient (in each caplet)

    Acetaminophen 500 mg

  • Purposes

    Pain reliever/fever reducer

  • Uses

     

    temporarily relieves minor aches and pains due to:
    headache
    backache
    muscular aches
    minor arthritis pain
    temporarily reduces fever
  • Warnings

    Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take

    more than 8 caplets in 24 hours, which is the maximum daily amount
    with other drugs containing acetaminophen
    3 or more alcoholic drinks every day while using this product

    Allergy alert: acetaminophen may cause severe skin reactions. Symptoms may include:

    skin reddening
    blisters
    rash

    If a skin reaction occurs, stop use and seek medical help right away.

    Do not use

    with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
    if you are allergic to acetaminophen or any of the inactive ingredients in this product

    Ask a doctor before use if you have

    liver disease

    Ask a doctor or pharmacist before use if you are

    taking the blood thinning drug warfarin

    Stop use and ask a doctor if

    pain gets worse or lasts more than 10 days
    fever gets worse or lasts more than 3 days
    redness or swelling is present
    any new symptoms appear

    These could be signs of a serious condition.

    If pregnant or breast-feeding,

    ask a health professional before use.

    Keep out of reach of children.

    Overdose warning:

    Taking more than the recommended dose can cause serious health problems. In case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

  • Directions

     

    do not take more than directed (see overdose warning)
    adults and children 12 years of age and over: take 2 caplets every 6 hours, while symptoms persist or as directed by a doctor
    do not take more than 8 caplets in 24 hours, unless directed by a doctor
    children under 12 years of age: ask a doctor
  • Other information

     

    each caplet contains: calcium 25 mg
    store below 30°C (86°F)
  • Inactive ingredients

    alginic acid, calcium carbonate, carnauba wax, colloidal silicon dioxide, crospovidone, hypromellose, magnesium stearate, polyethylene glycol, polysorbate 80, povidone, pregelatinized starch, sodium ethylparaben, sodium methylparaben, sodium propylparaben, titanium dioxide

  • Questions or comments?

    1-800-455-7139 (English/Spanish) weekdays

  • Principal Display Panel

    NDC 0135-0507-06

    Panadol®

    Advance

    WITH OPTI ZORB FORMULATION®

    ACETAMINOPHEN

    SEE NEW WARNINGS INFORMATION

    Pain Reliever

    Fever Reducer

    100 CAPLETS

    Tamper Evident Feature: Do not use if printed bottle seal (under cap) is missing or broken.

    READ AND KEEP CARTON FOR COMPLETE INFORMATION

    GlaxoSmithKline Consumer Healthcare, L.P.

    Moon Township, PA 15108

    Made in China

    ©2015 GSK

    All Rights Reserved.

    PANADOL, Beacon design, OPTIZORB and OPTIZORB design are registered trademarks of GSK group of companies.

    Keep Carton

    101997XB

    Panadol Advanced 100 count caplets carton
  • INGREDIENTS AND APPEARANCE
    PANADOL 
    acetaminophen tablet, film coated
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0135-0507
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 500 mg
    Inactive Ingredients
    Ingredient Name Strength
    ALGINIC ACID (UNII: 8C3Z4148WZ)  
    CALCIUM CARBONATE (UNII: H0G9379FGK)  
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CROSPOVIDONE (UNII: 68401960MK)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    POVIDONES (UNII: FZ989GH94E)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    SODIUM ETHYLPARABEN (UNII: Z0D00IVA10)  
    METHYLPARABEN SODIUM (UNII: CR6K9C2NHK)  
    PROPYLPARABEN SODIUM (UNII: 625NNB0G9N)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    Color WHITE Score 2 pieces
    Shape OVAL (caplet) Size 17mm
    Flavor   Imprint Code P
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0135-0507-02 50 in 1 CARTON 06/21/2011  
    1 NDC:0135-0507-01 2 in 1 PACKET; Type 0: Not a Combination Product    
    2 NDC:0135-0507-03 1 in 1 CARTON 06/21/2011  
    2   10 in 1 BOTTLE; Type 0: Not a Combination Product    
    3 NDC:0135-0507-04 1 in 1 CARTON 06/21/2011  
    3   20 in 1 BOTTLE; Type 0: Not a Combination Product    
    4 NDC:0135-0507-05 1 in 1 CARTON 06/21/2011  
    4   40 in 1 BOTTLE; Type 0: Not a Combination Product    
    5 NDC:0135-0507-06 1 in 1 CARTON 06/21/2011  
    5   100 in 1 BOTTLE; Type 0: Not a Combination Product    
     
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part343 06/21/2011 
  • 以下是“全球医药”详细资料
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