Active Ingredient (In Each 20.3 Ml)
Acetaminophen 650 mg
The following Structured Product Label (SPL) was submitted to the FDA by Pai Holdings, Llc Dba Pai Pharma for the product Acetaminophen (NDC 0121-3141). 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 20.3 ml), purposes, uses, do not use, stop use and ask a doctor if, directions, other information, questions or comments?, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Acetaminophen 650 mg
Pain reliever/fever reducer
• for the temporary relief of minor aches and pains due to
• for the minor pain from arthritis
• and to reduce fever
| age | dose |
|---|---|
| adults and children 12 years of age and over | 20.3 mL (650 mg) every 4 to 6 hours
not to exceed 6 doses in a 24-hour period |
| children under 12 years of age | consult a doctor |
■ Each 20.3 mL contains: sodium 24 mg
■ store at 20° to 25°C (68° to 77°F)
Call 1-800-845-8210. You may also report serious side effects to this phone number.
PAI Pharma
Greenville,SC 29605
www.paipharma.com
R05/25
Delivers 20.3 mL
NDC 0121-3141-21
Acetaminophen
Oral Solution USP
650 mg/20.3 mL
Pain Reliever/Fever Reducer
Alcohol Free/Dye Free/Sugar Free
Grape Flavored
Package Not Child-Resistant
Dist. by: PAI Pharma
GREENVILLE, SC 29605
See insert for drug facts
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