Pain Relief Extra Strength by Chain Drug Consortium
Medically reviewed on October 30, 2017
Dosage form: tablet
Ingredients: ACETAMINOPHEN 500mg
Labeler: Chain Drug Consortium
NDC Code: 68016-138
Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Acetaminophen 500 mg
temporary relief of minor aches and pains associated with common cold headache toothache
muscular aches backache arthritis menstrual cramps and reduction of fever
Liver warning: This product contains acetaminophen. Severe liver damage may occur if you takemore than 4000mg of acetaminophen in 24 hours with other drugs containing acetaminophen 3 or more alcoholic drinks every day while using 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
are taking the blood thinning drug warfarin
symptoms do not improve pain gets worse or lasts for more than 10 days ■ fever gets worse or lasts for more than 3 days new symptoms occur redness or swelling is present ■ a rare
sensitivity reaction occurs You may report side effects to 1-888-952-0050
ask a health professional before use
In case of accidental overdose, contact a doctor or Poison Control Center immediately. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms. Donot exceed recommended dosage.
Adults and children 12 years of age and older: Take 2 caplets (1,000 mg) every 6 hours while symptoms last. Do not take more than 6 caplets (3,000 mg) in 24 hours, unless directed by a doctor.
Children under 12 years of age: Do not use this extra strength product. This will provide more than the recommended dose (overdose) and could cause serious health problems.
corn starch, hydroxypropyl methylcellulose, polyethylene glycol, pregelatinized starch, stearic acid, titanium dioxide. May contain povidone, and sodium starch glycolates.
|Labeler - Chain Drug Consortium (101668460)|
|Registrant - Chain Drug Consortium (101668460)|
|A&Z Pharmaceutical, Inc.||926820705||LABEL(68016-138), MANUFACTURE(68016-138), PACK(68016-138), RELABEL(68016-138), REPACK(68016-138)|
Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.