Home > Pill Identifier > Excedrin Migraine (APAP 250 MG / ASA 250 MG / caffeine 65 MG) Oral Tablet

Pill Identifier Information of Excedrin Migraine (APAP 250 MG / ASA 250 MG / caffeine 65 MG) Oral Tablet

Drug Information

Excedrin Migraine (APAP 250 MG / ASA 250 MG / caffeine 65 MG) Oral Tablet

Imprint: E
Shape: C48336
Color: C48325
Ingredients: Acetaminophen; Aspirin; Caffeine
Size: 18.00
Score: 1
Rxtty: SY
Author: Novartis consumer Health, Inc.
Inactive Ingredients: BENZOIC ACID / CARNAUBA WAX / CELLULOSE, MICROCRYSTALLINE / FD&C BLUE NO. 1 / HYDROXYPROPYL CELLULOSE / HYPROMELLOSE / LIGHT MINERAL OIL / POLYSORBATE 20 / COPOVIDONE / POVIDONE / PROPYLENE GLYCOL / SORBITAN MONOLAURATE / TITANIUM DIOXIDE>

Complete Information

  • Active ingredient (in each caplet)

    Acetaminophen 250 mg

    Aspirin 250 mg (NSAID*)

    Caffeine 65 mg

    *nonsteroidal anti-inflammatory drug

  • Purposes

    Pain reliever

    Pain reliever

    Pain reliever aid

  • Uses

    •
    temporarily relieves minor aches and pains due to:
    o
    headache
    o
    a cold
    o
    arthritis
    o
    muscular aches
    o
    toothache
    o
    premenstrual & menstrual cramps
  • Warnings

    Reye’s syndrome: Children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use this product. When using this product, if changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of Reye’s syndrome, a rare but serious illness.

    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.

    Allergy alert: Aspirin may cause a severe allergic reaction which may include:

    •
    hives
    •
    facial swelling
    •
    asthma (wheezing)
    •
    shock

    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

    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

    Caffeine warning: The recommended dose of this product contains about as much caffeine as a cup of coffee. Limit the use of caffeine-containing medications, foods, or beverages while taking this product because too much caffeine may cause nervousness, irritability, sleeplessness, and, occasionally, rapid heart beat.

    Do not use
    •
    if you have ever had an allergic reaction to acetaminophen, aspirin or any other pain reliever/fever reducer
    •
    with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.

    Ask a doctor before use if
    •
    you have liver disease
    •
    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 are taking a diuretic
    •
    you have asthma

    Ask a doctor or pharmacist before use if you are taking
    •
    a prescription drug for diabetes, gout, or arthritis
    •
    any other drug, or are under a doctor’s care for any serious condition

    Keep out of reach of children.

    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 use more than directed
    •
    drink a full glass of water with each dose
    •
    adults and children 12 years and over: take 2 caplets every 6 hours; not more than 8 caplets in 24 hours
    •
    children under 12 years: ask a doctor
  • Other information

    •
    store at 20°- 25°C (68°- 77°F)
    •
    close cap tightly after use
    •
    read all product information before using. Keep this box for important information
  • Inactive ingredients

    benzoic acid, carnauba wax, FD&C blue #1, hydroxypropylcellulose, hypromellose, light mineral oil, microcrystalline cellulose, polysorbate 20, povidone, propylene glycol, simethicone emulsion, sorbitan monolaurate, stearic acid, titanium dioxide

  • Questions or comments?

    1-800-452-0051

  • Principal Display Panel

    NDC 0067-2000-10

    EXCEDRIN®

    EXTRA STRENGTH

    Acetaminophen, Aspirin (NSAID) and Caffeine

    Pain Reliever/Pain Reliever Aid

    10 CAPLETS

    TAMPER-EVIDENT BOTTLE

    DO NOT USE IF INNER FOIL SEAL INPRINTED WITH “SEALED for YOUR PROTECTION” IS BROKEN OR MISSING

    Distributed by: GSK Consumer Healthcare

    Warren, NJ 07059

    ©2015 GSK or its licensor.

    Visit us at www.excedrin.com

    46172146

    46172146_Excedrin Extra Strength caplets_10 ct.JPG
  • INGREDIENTS AND APPEARANCE
    EXCEDRIN  EXTRA STRENGTH PAIN RELIEVER
    acetaminophen, aspirin (nsaid), and caffeine tablet, film coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0067-2000
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN250 mg
    ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN250 mg
    CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E) CAFFEINE65 mg
    Inactive Ingredients
    Ingredient NameStrength
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    LIGHT MINERAL OIL (UNII: N6K5787QVP)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorWHITE (White) Scoreno score
    ShapeCAPSULE (Capsule-Shaped Tablet) Size18mm
    FlavorImprint Code E
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0067-2000-022 in 1 POUCH; Type 0: Not a Combination Product09/27/2006
    2NDC:0067-2000-101 in 1 CARTON09/27/2006
    210 in 1 BOTTLE; Type 0: Not a Combination Product
    3NDC:0067-2000-241 in 1 CARTON09/27/2006
    324 in 1 BOTTLE; Type 0: Not a Combination Product
    4NDC:0067-2000-301 in 1 CARTON09/27/2006
    430 in 1 BOTTLE; Type 0: Not a Combination Product
    5NDC:0067-2000-501 in 1 CARTON09/27/2006
    550 in 1 BOTTLE; Type 0: Not a Combination Product
    6NDC:0067-2000-911 in 1 CARTON09/27/2006
    6100 in 1 BOTTLE; Type 0: Not a Combination Product
    7NDC:0067-2000-94100 in 1 BOTTLE; Type 0: Not a Combination Product09/27/200612/31/2014
    8NDC:0067-2000-831 in 1 CARTON09/27/2006
    8125 in 1 BOTTLE; Type 0: Not a Combination Product
    9NDC:0067-2000-201 in 1 CARTON09/27/2006
    9200 in 1 BOTTLE; Type 0: Not a Combination Product
    10NDC:0067-2000-771 in 1 CARTON09/27/2006
    10250 in 1 BOTTLE; Type 0: Not a Combination Product
    11NDC:0067-2000-07250 in 1 BOTTLE; Type 0: Not a Combination Product09/27/200612/31/2014
    12NDC:0067-2000-331 in 1 CARTON09/27/2006
    12300 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01309/27/2006
    Labeler - Haleon US Holdings LLC (079944263)
© 2026 - Pharmaguru.com. All rights reserved.