The labeling of all systemic drug products intended for human use indicated to treat a bacterial infection, except a mycobacterial infection, must bear the following statements:
(a)
At the beginning of the label, under the product name, the labeling must state:
(b)
In the “Indications and Usage” section, the labeling must state:
(c)
In the “Precautions” section, under the “General” subsection, the labeling must state:
(d)
In the “Precautions” section, under the “Information for Patients” subsection, the labeling must state:
Code of Federal Regulations
[68 FR 6081, Feb. 6, 2003]