Active Ingredient (In Each Tablet)
Acetaminophen 500 mg
The following Structured Product Label (SPL) was submitted to the FDA by Proficient Rx Lp for the product Pharbetol (NDC 71205-478). 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 tablet), purpose, uses, warnings, do not use, ask a doctor before use if you have, ask a doctor or pharmacist before use if you are, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Acetaminophen 500 mg
Pain reliever/fever reducer
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.
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)
adult and children 12 years and over |
|
children under 12 years | Ask a doctor |
povidone, pregelatinized corn starch, sodium starch glycolate, stearic acid
Adverse drug event call: 1-866-562-2756 Mon - Fri: 8 AM to 4 PM
Repackaged By:
Proficient Rx LP
Thousand Oaks, CA 91320
NDC 71205-478-24
manufactured in the USA
Extra Strength *Compare to the active ingredient in Extra Strength Tylenol® Caplet
Do not use with any other product containing acetaminophen
PHARBETOL
Acetaminophen 500mg
Pain Reliever • Fever Reducer
24 TABLETS
* Please review the disclaimer below.