Vermont § 4064 - Misbranded drugs or device A drug or device is misbranded:

§ 4064. Misbranded drugs or device A drug or device is misbranded:

• (1) If its labeling is false or misleading in any particular. (2) If in package form unless it bears a label containing: (A) the name and place of business of the manufacturer, packer, or distributor; and (B) an accurate statement of the quantity of the contents in terms of weight, measure,
  or numerical count, provided that under this subdivision (B) reasonable variations
  shall be permitted, and exemptions as to small packages shall be established by rules
  adopted by the Department. (3) If any word, statement, or other information required by or under authority of this
  chapter to appear on the labeling is not prominently placed thereon with such conspicuousness
  (as compared with other words, statements, designs, or devices in the labeling) and
  in such terms as to render it likely to be read and understood by the ordinary individual
  under customary conditions of purchase and use. (4) If it is for use by humans and contains any quantity of the narcotic or hypnotic substance
  alpha-eucaine, barbituric acid, beta-eucaine, bromal, cannabis, carbromal, chloral,
  coca, cocaine, codeine, heroin, morphine, opium, paraldehyde, peyote, sulphonmethane,
  or other recognized narcotic or hypnotic substances or any chemical derivative of
  those substances, which derivative has been by the Department, after investigation,
  found to be, and by rules under this chapter, designated as habit forming, unless
  its label bears the name and quantity or proportion of the substance or derivative
  and in juxtaposition therewith the statement “warning—may be habit forming.” (5) If it is a drug and is not designated solely by a name recognized in an official compendium
  unless its label bears: (A) the common or usual name of the drug, if such there be; and (B) in case it is fabricated from two or more ingredients, the common or usual name of
  each active ingredient, including the kind and quantity or proportion of any alcohol,
  and also including whether active or not the name and quantity or proportion of any
  bromides, ether, chloroform, acetanilid, acetphenetidin, amidopyrine, antipyrine,
  atropine, hyoscine, hyoscyamine, arsenic, digitalis, glucosides, mercury, ouabain,
  strophanthin, strychnine, thyroid, or other synthetic compounds, or any derivative
  or preparation of any of those substances, contained therein, provided that to the
  extent that compliance with the requirements of this subdivision (B) is impracticable,
  exemptions shall be established by rules adopted by the Department. (6) Unless its labeling bears: (A) adequate directions for use; and (B) such adequate warnings against use in those pathological conditions or by children
  where its use may be dangerous to health, or against unsafe dosage or methods or duration
  of administration or application, in such manner and form, as are necessary for the
  protection of users, provided that where any requirement of this subsection, as applied
  to any drug or device, is not necessary for the protection of the public health, the