Active Ingredient (In Each Gelcap)
Acetaminophen USP, 500 mg
The following Structured Product Label (SPL) was submitted to the FDA by Walmart for the product Acetaminophen (NDC 79903-269). 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 ingredient (in each gelcap), purpose, uses, liver warning:, allergy alert:, do not use, ask a doctor before use if you have, ask a doctor or pharmacist before use if you are, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Acetaminophen USP, 500 mg
Pain reliever/fever reducer
This product contains acetaminophen. Severe liverdamage may occur if you take
acetaminophen may cause severe skin reactions. Symptoms may include:
If a skin reaction occurs, stop use and seekmedical help right away
acetaminophen, ask a doctor or pharmacist.
liver disease
taking the blood thinning drug warfarin
These could be signs of a serious condition
ask a health professional before use
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.
adults and children 12 years and over
children under 12 years
ammonium hydroxide, black iron oxide, colloidal silicon dioxide, croscarmellose sodium, D&C red #33, FD&C blue #1, FD&C red #40,
FD&C yellow #6, gelatin, hydroxypropyl cellulose, hypromellose, isopropyl alcohol, n-butyl alcohol, polyethylene glycol, povidone k-30,
pregelatinized starch, propylene glycol, red iron oxide, shellac glaze, stearic acid, titanium dioxide, yellow iron oxide
1-888-287-1915
* Please review the disclaimer below.