Otc - Questions
Questions (Questions)
Extra Strength Acetaminophen
FDA Label NDC 69732-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hi-tech Nutraceuticals, Llc for the product Extra Strength Acetaminophen (NDC 69732-001). 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 otc - active ingredient, otc - ask doctor, otc - ask doctor/pharmacist, otc - do not use, otc - keep out of reach of children, otc - pregnancy or breast feeding, otc - purpose, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - When Using
Directions (Directions)
Warnings
Warnings (Warnings)
Indications & Usage
Uses (Uses)
Dosage & Administration
Uses:
■ temporarily relieves minor aches and pains due to:
■ the common cold ■ headache ■backache
■ minor pain of arthritis ■ toothache ■ muscular aches
■ premenstrual and menstrual cramps
■ temporarily reduces fever
Package Label.Principal Display Panel
Front Label (Front)
* Please review the disclaimer below.
