Drug Factsactive Ingredient
Acetaminophen 500 mg
The following Structured Product Label (SPL) was submitted to the FDA by Shield Pharmaceuticals Corp for the product Pain Reliever (NDC 83059-0103). 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 drug factsactive ingredient, purpose, uses, warnings, otc - do not use, otc - ask doctor, otc - ask doctor/pharmacist, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Acetaminophen 500 mg
Pain reliever/fever reducer
temporarily relieves minor aches and pains due to:
Liver warning
This product contains acetaminophen. Severe liver damage may occur if you take
Allergy alert:acetaminophen may cause severe skin reactions. Symptoms may include:
If a skin reaction occurs, stop use and seek medical help right away.
Do not use
Ask a doctor before use if youhave liver disease
Ask a doctor or pharmacist before use if you aretaking the blood thinning drug warfarin
Stop use and ask a doctor if
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.
Overdose warning
In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222). Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.
do not take more than directed (see overdose warning)
| adults and children 12 years and over |
|
| children under 12 years | ask a doctor |
store between 20-25°C (68-77°F)
magnesium stearate, potassium sorbate, povidone (K30), pregelatinized starch, purified water, sodium starch glycolate
1-800-373-6981
Compare to the active ingredient
in Tylenol® Extra Strength
Pain Reliever
Acetaminophen 500 mg
* Please review the disclaimer below.