Acetaminophen 250 Mg And Ibuprofen 125 Mg Tablet, Film Coated
FDA Label NDC 25000-080

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Marksans Pharma Limited for the product Acetaminophen 250 Mg And Ibuprofen 125 Mg (NDC 25000-080). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredients (in each caplet), purposes, uses, warnings, do not use, ask a doctor before use if, ask a doctor or pharmacist before use if you are, when using this product, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients (In Each Caplet)

Acetaminophen 250 mg
Ibuprofen 125 mg (NSAID*)
*nonsteroidal anti-inflammatory drug

Purposes

Pain reliever
Pain reliever


Uses

• temporarily relieves minor aches and pains due to:
o headache
o toothache
o backache
o menstrual cramps
o muscular aches
o minor pain of arthritis


Warnings

Acetaminophen liver damage warning:
This product contains acetaminophen. Severe liver damage may occur if you take:
• with other drugs containing acetaminophen
• more than 6 caplets in 24 hours, which is the maximum daily amount for this product
• 3 or more alcoholic drinks every day while using this product


Acetaminophen allergy alert: may cause severe skin reactions. Symptoms may include:
• skin reddening
• blisters
• rash
If skin reaction occurs, stop use and seek medical help right away.


NSAID 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 and seek medical help right away.


NSAID 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

• 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 have ever had an allergic reaction to acetaminophen or any other pain reliever
• right before or after heart surgery

Ask A Doctor Before Use If

• you have liver disease
• stomach bleeding warning applies to you
• you have problems or serious side effects from taking pain relievers
• you have a history of stomach problems, such as heartburn
• you have high blood pressure, heart disease, liver cirrhosis, kidney disease, asthma, or had a stroke
• you are taking a diuretic


Ask A Doctor Or Pharmacist Before Use If You Are

• under a doctor’s care for any serious condition
• taking aspirin for heart attack or stroke, because ibuprofen may decrease this benefit of aspirin
• taking any other drug

When Using This Product

• take with food or milk if stomach upset occurs

Stop Use And Ask A Doctor If

• you experience any of the following signs of stomach bleeding:
o feel faint
o vomit blood
o have bloody or black stools
o have stomach pain that does not get better
• you have symptoms of heart problems or stroke:
o chest pain
o trouble breathing
o weakness in one part or side of body
o slurred speech
o leg swelling
• pain gets worse or lasts more than 10 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 (1-800-222-1222). Prompt 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

adults and children 12 years and over   • take 2 caplets every 8 hours while symptoms persist
children under 12 years • ask a doctor

 • do not take more than 6 caplets in 24 hours, unless directed by a doctor



Other Information

• read all warnings and directions before use. Keep carton.
• store at 20-25°C (68-77°F)
• avoid excessive heat above 40°C (104°F)


Inactive Ingredients

colloidal anhydrous silica, corn starch, croscarmellose sodium, glyceryl dibehenate, hypromellose, microcrystalline cellulose, polydextrose, povidone, red iron oxide, titanium dioxide, triacetin, yellow iron oxide

Questions Or Comments?

Call 1-877-376-4271 (weekdays 9 AM to 5 PM)



Distributed by:

Time-Cap Labs, Inc.
7 Michael Avenue,
Farmingdale,
NY 11735, USA


Made in India

Principal Display Panel

NDC 25000-080-72

Acetaminophen 250 mg and Ibuprofen 125 mg Tablets

18 count carton label


Ibupara-ifc-label-18s (Ibupara Ifc Label 18s)

Ibupara-ifc-label-18s (Ibupara Ifc Label 18s)



NDC 25000-080-72

Acetaminophen 250 mg and Ibuprofen 125 mg Tablets

18 count bottle label

18s Label (Ibupara Bottle Label 18s)

18s Label (Ibupara Bottle Label 18s)

 


NDC 25000-080-07

Acetaminophen 250 mg and Ibuprofen 125 mg Tablets

90 count carton label


Ibupara-ifc-label-90s (Ibupara Ifc Label 90s)

Ibupara-ifc-label-90s (Ibupara Ifc Label 90s)



NDC 25000-080-07

Acetaminophen 250 mg and Ibuprofen 125 mg Tablets

90 count bottle label

90s Label (Ibupara Bottle Label 90s)

90s Label (Ibupara Bottle Label 90s)

 


NDC 25000-080-74

Acetaminophen 250 mg and Ibuprofen 125 mg Tablets

288 count bottle label


288s Label (Ibupara Bottle Label 288s)

288s Label (Ibupara Bottle Label 288s)

 



 


* Please review the disclaimer below.