Active Ingredient (In Each Tablet)
Acetaminophen 325 mg
The following Structured Product Label (SPL) was submitted to the FDA by Ulai Health Llc for the product Pharbetol (NDC 73057-353). 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 325 mg
Pain reliever/fever reducer
Liver warning: This product contains acetaminophen. The maximum daily dose of this product is 10 tablets (3,250 mg) in 24 hours for adults or 5 tablets (1,625 mg) in 24 hours for children. Severe liver damage may occur if
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).
| adults and children 12 years and over |
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| children 6 to under 12 years |
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| children under 6 years | ask a doctor |
povidone, pregelatinized corn starch, sodium starch glycolate, stearic acid
(866) 562-2756 (Mon - Fri 8 AM to 4 PM EST)
PHARBEST
NDC 73057-353-11
Manufactured in the USA
Regular Strength *COMPARE TO the active ingredient in TYLENOL® Regular Strength
Contains no Aspirin
PHARBETOL
Acetaminophen 325 mg each
Pain Reliever/Fever Reducer
1000 TABLETS
* Please review the disclaimer below.