ARTICLE 3. Misbranded Drugs or Devices

Article 3 added by Stats. 1995, Ch. 415, Sec. 6.

§§ 111330–111510 · 35 sections

§ 111330 Any drug or device is misbranded if its labeling is false or misleading in any particular.
§ 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).
§ 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 manufacturer,…
§ 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 labeling is not…
§ 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…
§ 111360 Any drug subject to Section 111470 is misbranded unless the manufacturer, packer, or distributor of the drug includes, in all advertisements and other…
§ 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…
§ 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…
§ 111376 (a) The department may adopt regulations relating to brand name or generic mifepristone or any drug used for medication abortion by including brand name or…
§ 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 as prescribed in the…
§ 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 form and manner…
§ 111390 Any drug or device is misbranded if its container is so made, formed, or filled as to be misleading.
§ 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 name of another drug. (c)…
§ 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 chain…
§ 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, or suggested…
§ 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 packaging and labeling fail to…
§ 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 the trademark,…
§ 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.
§ 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 the…
§ 111435 Any drug is misbranded if its packaging or labeling is in violation of an applicable regulation issued pursuant to Section 108685 or 108700.
§ 111440 It is unlawful for any person to manufacture, sell, deliver, hold, or offer for sale any drug or device that is misbranded.
§ 111445 It is unlawful for any person to misbrand any drug or device.
§ 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 drug or device.
§ 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 device if the act results…
§ 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) It accords…
§ 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 and Drug Administration…
§ 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 law to prescribe…
§ 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 device being misbranded while held for…
§ 111480 (a) A drug or device sold by filling or refilling a written or oral prescription of a practitioner licensed to prescribe the drug or device shall be exempt…
§ 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…
§ 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 the statement “Caution:…
§ 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 now…
§ 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…
§ 111505 For purposes of Section 111510, the following definitions shall apply: (a) “Distributor” means any corporation, person, or other entity, not engaged in the…
§ 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 with a code imprint…