Pain Reliever Extra Strength 500 mg/1

Acetaminophen · TABLET, FILM COATED · L.N.K. International, Inc.

No Recall HistoryCurrently in Shortage

Plain English

Pain Reliever Extra Strength is a tablet, film coated containing acetaminophen at 500 mg/1, taken oral. Manufactured by L.N.K. International, Inc..

Key Facts

Brand Name: Pain Reliever Extra Strength
Generic Name: Acetaminophen
NDC Code (Product): 50844-175
Manufacturer: L.N.K. International, Inc.
Strength: 500 mg/1
Dosage Form: TABLET, FILM COATED
Route: ORAL
Marketing Status
Application #: M013
Marketing Start: 04/02/1993

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

off label use22,401 reports

fatigue20,447 reports

drug ineffective18,172 reports

pain18,115 reports

nausea17,637 reports

headache16,730 reports

toxicity to various agents15,548 reports

dyspnoea14,586 reports

arthralgia14,315 reports

pyrexia14,274 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses temporarily relieves minor aches and pains due to: headache the common cold backache minor pain of arthritis toothache muscular aches premenstrual and menstrual cramps temporarily reduces fever

Dosage & Administration

Directions do not take more than directed adults and children 12 years and over take 2 gelcaps every 6 hours while symptoms last do not take more than 6 gelcaps in 24 hours, unless directed by a doctor do not take for more than 10 days unless directed by a doctor children under 12 years: ask a doctor

Warnings

Warnings Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take more than 4,000 mg of acetaminophen in 24 hours 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 if you are allergic to acetaminophen or any of the inactive ingredients in this product 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. Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin. Stop use and ask a doctor if new symptoms occur pain gets worse or lasts more than 10 days fever gets worse or lasts more than 3 days redness or swelling is present 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. In case of overdose, get medical help or cont…

Frequently Asked Questions

What is Pain Reliever Extra Strength used for?

Pain Reliever Extra Strength contains Acetaminophen. It is a tablet, film coated taken oral. Consult your doctor for specific uses.

Is Pain Reliever Extra Strength a controlled substance?

Pain Reliever Extra Strength is not classified as a controlled substance by the DEA.

What is the generic name for Pain Reliever Extra Strength?

The generic name for Pain Reliever Extra Strength is Acetaminophen. There are 12 other brand versions of Acetaminophen.

What is the NDC code for Pain Reliever Extra Strength 500 mg/1?

The NDC (National Drug Code) for Pain Reliever Extra Strength 500 mg/1 is 50844-175, listed by L.N.K. International, Inc..

Product NDC

50844-175

Package NDC

50844-175-12

Other Acetaminophen Brands

See all →

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)