California Health and Safety Code ARTICLE 3 - Misbranded Drugs or Devices

• Section 111330.
  Any drug or device is misbranded if its labeling is false or misleading in any particular.(Amended by Stats. 2000, Ch. 796, Sec. 7. Effective January...
• Section 111335.
  Any drug or device is misbranded if its labeling or packaging does not conform to the requirements of Chapter 4 (commencing with Section 110290).(Added by...
• Section 111340.
  Any drug or device is misbranded unless it bears a label containing all of the following information:(a)  The name and place of business of the...
• Section 111345.
  Any drug or device is misbranded if any word, statement, or other information required by or under this part to appear on the label or...
• Section 111355.
  (a)  Any drug is misbranded unless its label bears, to the exclusion of any other nonproprietary name except the applicable, systematic chemical name or the...
• Section 111360.
  Any drug subject to Section 111470 is misbranded unless the manufacturer, packer, or distributor of the drug includes, in all advertisements and other descriptive matter...
• Section 111365.
  Any drug subject to Section 111470 is misbranded unless the established name of the prescription drug or prescription drug ingredient is printed on the label...
• Section 111375.
  Any drug or device is misbranded unless its labeling bears all of the following information:(a)  Adequate directions for use. (b)  Such adequate warnings against use...
• Section 111380.
  Any drug is misbranded if it purports to be a drug that is recognized in an official compendium and it is not packaged and labeled...
• Section 111385.
  Any drug or device is misbranded if the department determines that the drug or device is liable to deterioration, unless it is packaged in that...
• Section 111390.
  Any drug or device is misbranded if its container is so made, formed, or filled as to be misleading.(Added by Stats. 1995, Ch. 415, Sec....
• Section 111395.
  Any drug is misbranded in any of the following cases:(a)  It is an imitation of another drug. (b)  It is offered for sale under the...
• Section 111397.
  (a) Any foreign dangerous drug that is not approved by the United States Food and Drug Administration or that is obtained outside of the licensed supply...
• Section 111400.
  Any drug or device is misbranded if it is dangerous to health when used in the dosage, or with the frequency or duration prescribed, recommended,...
• Section 111415.
  Any drug is misbranded if it is a color additive, intended for use in or on drugs for the purpose of coloring only and its...
• Section 111420.
  A drug or device is misbranded if a trademark, trade name, or other identifying mark, imprint, or device of another person, or any likeness of...
• Section 111425.
  A drug or device is misbranded if it was manufactured in this state in an establishment not duly licensed as provided in this part.(Added by...
• Section 111430.
  A drug or device is misbranded if it was manufactured in an establishment not duly registered with the Secretary of Health, Education, and Welfare of...
• Section 111435.
  Any drug is misbranded if its packaging or labeling is in violation of an applicable regulation issued pursuant to Section 108685 or 108700.(Added by Stats....
• Section 111440.
  It is unlawful for any person to manufacture, sell, deliver, hold, or offer for sale any drug or device that is misbranded.(Added by Stats. 1995,...
• Section 111445.
  It is unlawful for any person to misbrand any drug or device.(Added by Stats. 1995, Ch. 415, Sec. 6. Effective January 1, 1996.)
• Section 111450.
  It is unlawful for any person to receive in commerce any drug or device that is misbranded or to deliver or proffer for delivery any...
• Section 111455.
  It is unlawful for any person to alter, mutilate, destroy, obliterate, or remove the label or any part of the labeling of any drug or...
• Section 111460.
  Any drug or device intended for export shall not be deemed to be misbranded under this part if it satisfies all of the following requirements:(a)...
• Section 111465.
  A drug or device is deemed misbranded under the laws of this state if it is subject to regulations issued by the United States Food...
• Section 111470.
  The following drugs or devices, that are intended for use by man, shall be sold only upon a written prescription of a practitioner licensed by...
• Section 111475.
  The act of selling a drug or device contrary to Section 111470 shall be deemed to be an act that results in the drug or...
• Section 111480.
  Any drug or device sold by filling or refilling a written or oral prescription of a practitioner licensed to prescribe the drug or device shall...
• Section 111485.
  The department may, by regulation, remove any drug or device subject to Sections 111350 and 111550 from the requirements of Section 111470, when the requirements...
• Section 111490.
  (a)  A drug or device that is subject to Section 111470 is misbranded if at any time prior to dispensing, its label fails to bear...
• Section 111495.
  Nothing in this article shall be construed to relieve any person from any requirement prescribed by or under authority of law with respect to drugs...
• Section 111500.
  A physician, dentist, podiatrist, or veterinarian may personally furnish his or her own patient with drugs as are necessary in the treatment of the condition...
• Section 111505.
  For purposes of Section 111510, the following definitions shall apply:(a)  “Distributor” means any corporation, person, or other entity, not engaged in the manufacture of a...
• Section 111510.
  (a)  No legend drug in solid dosage form may be manufactured or distributed for sale in this state unless it is clearly marked or imprinted...

Last modified: October 22, 2018