Active Ingredients
Acetaminophen 325 mg
Regular Strength Pain Relief
FDA Label NDC 66267-999
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Nucare Pharmaceuticals,inc. for the product Regular Strength Pain Relief (NDC 66267-999). 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 ingredients, purpose, uses, warnings, otc - keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Pain Reliever/Fever Reducer
Uses
- temporarily relieves minor aches and pains
- temporarily reduces fever
Warnings
Liver warning:
This product contains acetaminophen. Severe liver damage may occur if you take
Do not use
Ask a doctor before use
if you have liver disease
.
Ask a doctor or pharmacist before use if you
are taking the blood thinning drug warfarin.
Stop use and ask a doctor if
- more than 12 tablets in 24 hours, which is the maximum daily amount
- with other drugs containing acetaminophen
- 3 or more alcoholic drinks every day while using this product
- with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
These could be signs of a serious condition.
If pregnant or breast-feeding,
ask a health professional before use.
Overdose Warning:Taking more than the recommended dose (overdose) may cause liver damage. In case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.
- pain gets worse or lasts more than 10 days
- fever gets worse or lasts more than 3 days
- new symptom occur
- redness or swelling is present
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Directions
- do not take more than directed
- adults and children 12 years and over: take 2 tablets every 4-6 hours, as needed; not more than 12 tablets in 24 hours
- children under 12 years: ask a doctor
Other Information
- TAMPER EVIDENT: Do not use if imprinted seal under cap is missing or broken.
- store at 20⁰C-25⁰C (68⁰F-77⁰F)
- for institutional use only
Inactive Ingredients
povidone, sodium starch glycolate, starch stearic acid. May also contain: crospovidone, methylparaben and probylparaben
Package Label
Pdp (66267 999 00 G58)
* Please review the disclaimer below.
