NDC | 0067-2039-02, 0067-2039-07, 0067-2039-08, 0067-2039-09, 0067-2039-24, 0067-2039-30, 0067-2039-33, 0067-2039-50, 0067-2039-77, 0067-2039-83, 0067-2039-84, 0067-2039-86, 0067-2039-91, 0067-2039-92, 0067-2039-94 |
Set ID | 7ed841fb-a61c-4868-b4e5-4f2311a5e79c |
Category | HUMAN OTC DRUG LABEL |
Packager | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC |
Generic Name | |
Product Class | |
Product Number | |
Application Number | NDA020802 |
- Active ingredients (in each caplet)
- Purpose
- Uses
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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:
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- skin reddening
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- blisters
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- 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:
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- hives
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- facial swelling
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- asthma (wheezing)
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- shock
Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take
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- more than 2 caplets in 24 hours, which is the maximum daily amount
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- with other drugs containing acetaminophen
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- 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
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- are age 60 or older
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- have had stomach ulcers or bleeding problems
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- take a blood thinning (anticoagulant) or steroid drug
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- take other drugs containing prescription or nonprescription NSAIDs (aspirin, ibuprofen, naproxen, or others)
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- have 3 or more alcoholic drinks every day while using this product
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- take more or for a longer time than directed
Medication overuse headache warning: Headaches may worsen if this product is used for 10 or more days per month.
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
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- if you have ever had an allergic reaction to acetaminophen, aspirin or any other pain reliever/fever reducer
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- 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 doctor before use if
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- you have never had migraines diagnosed by a health professional
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- you have a headache that is different from your usual migraines
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- you have the worst headache of your life
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- you have fever and stiff neck
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- you have headaches beginning after or caused by head injury, exertion, coughing or bending
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- you experienced your first headache after the age of 50
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- you have daily headaches
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- you have a migraine so severe as to require bed rest
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- you have liver disease
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- stomach bleeding warning applies to you
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- you have a history of stomach problems, such as heartburn
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- you have high blood pressure, heart disease, liver cirrhosis, or kidney disease
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- you are taking a diuretic
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- you have asthma
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- you have problems or serious side effects from taking pain relievers or fever reducers
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- you have vomiting with your migraine headache
Ask a doctor or pharmacist before use if you are
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- taking a prescription drug for:
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- diabetes
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- gout
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- arthritis
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- under a doctor’s care for any serious condition
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- taking any other drug
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- taking any other product that contains aspirin, acetaminophen, or any other pain reliever/fever reducer
Stop use and ask a doctor if
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- an allergic reaction occurs. Seek medical help right away.
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- you experience any of the following signs of stomach bleeding:
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- feel faint
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- vomit blood
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- have bloody or black stools
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- have stomach pain that does not get better
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- your migraine is not relieved or worsens after first dose
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- new or unexpected symptoms occur
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- ringing in the ears or loss of hearing occurs
- Directions
- Other information
- Inactive Ingredients
- Questions or comments?
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Principal Display Panel
NDC 0067-2039-24
See new warnings information
EXCEDRIN®
MIGRAINE
Acetaminophen, Aspirin (NSAID) and Caffeine
Pain Reliever/Pain Reliever Aid
24
CAPLETS*
*CAPSULE-SHAPED TABLETS
TAMPER-EVIDENT BOTTLE
DO NOT USE IF INNER FOIL SEAL IMPRINTED WITH “SEALED for YOUR PROTECTION” IS BROKEN OR MISSING
Distributed by: GSK Consumer Healthcare, Warren, NJ 07059
©2017 GSK or its licensor.
Visit us at www.excedrin.com
62000000012933
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INGREDIENTS AND APPEARANCE
EXCEDRIN MIGRAINE
acetaminophen, aspirin (nsaid) and caffeine tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0067-2039 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 250 mg ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN 250 mg CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E) CAFFEINE 65 mg Inactive Ingredients Ingredient Name Strength BENZOIC ACID (UNII: 8SKN0B0MIM) CARNAUBA WAX (UNII: R12CBM0EIZ) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) LIGHT MINERAL OIL (UNII: N6K5787QVP) POLYSORBATE 20 (UNII: 7T1F30V5YH) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SORBITAN MONOLAURATE (UNII: 6W9PS8B71J) STEARIC ACID (UNII: 4ELV7Z65AP) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color WHITE (White) Score no score Shape CAPSULE (Capsule shaped tablet) Size 18mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0067-2039-02 2 in 1 POUCH; Type 0: Not a Combination Product 02/15/2010 2 NDC:0067-2039-08 1 in 1 CARTON 02/15/2010 12/31/2014 2 8 in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:0067-2039-09 1 in 1 CARTON 02/15/2010 07/31/2017 3 10 in 1 BOTTLE; Type 0: Not a Combination Product 4 NDC:0067-2039-24 1 in 1 CARTON 02/15/2010 4 24 in 1 BOTTLE; Type 0: Not a Combination Product 5 NDC:0067-2039-30 1 in 1 CARTON 02/15/2010 5 30 in 1 BOTTLE; Type 0: Not a Combination Product 6 NDC:0067-2039-50 1 in 1 CARTON 02/15/2010 6 50 in 1 BOTTLE; Type 0: Not a Combination Product 7 NDC:0067-2039-94 100 in 1 BOTTLE; Type 0: Not a Combination Product 02/15/2010 12/31/2012 8 NDC:0067-2039-91 1 in 1 CARTON 02/15/2010 8 100 in 1 BOTTLE; Type 0: Not a Combination Product 9 NDC:0067-2039-83 1 in 1 CARTON 02/15/2010 9 125 in 1 BOTTLE; Type 0: Not a Combination Product 10 NDC:0067-2039-84 125 in 1 BOTTLE; Type 0: Not a Combination Product 02/15/2010 07/31/2014 11 NDC:0067-2039-86 1 in 1 CARTON 02/15/2010 12/31/2014 11 125 in 1 BOTTLE; Type 0: Not a Combination Product 12 NDC:0067-2039-92 1 in 1 CARTON 02/15/2010 12 200 in 1 BOTTLE; Type 0: Not a Combination Product 13 NDC:0067-2039-77 1 in 1 CARTON 02/15/2010 13 250 in 1 BOTTLE; Type 0: Not a Combination Product 14 NDC:0067-2039-07 250 in 1 BOTTLE; Type 0: Not a Combination Product 02/15/2010 12/31/2012 15 NDC:0067-2039-33 1 in 1 CARTON 02/15/2010 15 300 in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA020802 02/15/2010 Labeler - GlaxoSmithKline Consumer Healthcare Holdings (US) LLC (079944263)