California

Health and Safety Code - HSC

17,661 sections, each with the official text and a plain-English explanation of what it means for you.

• § 108985.6 — (a) A violation of Chapter 14 (commencing with Section 108980) for the unlawful manufacturing, selling, delivering, holding, or offering for sale in commerce of a cosmetic product containing any of th
• § 108985.7 — (a) (1) The Combating Unsafe ReLaxers (C.
• § 109000 — (a) For purposes of this article, the following terms have the following definitions: (1) “Food packaging” means a nondurable package, packaging component, or food service ware that is intended to con
• § 109010 — For purposes of this article, the following terms have the following definitions: (a) “Cookware” means durable houseware items that are used in homes and restaurants to prepare, dispense, or store foo
• § 109011 — (a) Commencing on January 1, 2024, a manufacturer of cookware sold in the state that contains one or more intentionally added chemicals present on the designated list in the handle of the product or i
• § 109012 — Commencing on January 1, 2023, a manufacturer of cookware sold in the state that contains one or more intentionally added chemicals present on the designated list in the handle of the product or in an
• § 109013 — Commencing on January 1, 2023, on the internet website for the cookware, and on January 1, 2024, on the cookware package, a manufacturer shall not make a claim that the cookware is free of any specifi
• § 109014 — Cookware that contains one or more intentionally added chemicals present on the designated list in the handle of the product or in any product surface that comes into contact with food, foodstuffs, or
• § 109020 — For purposes of this chapter, the following definitions apply: (a) “Compact fluorescent lamp” means a compact low-pressure, mercury-containing, electric-discharge light source in which a fluorescent c
• § 109021 — (a) On and after January 1, 2024, a screw or bayonet base type compact fluorescent lamp shall not be offered for final sale, sold at final sale, or distributed in this state as a new manufactured prod
• § 109022 — This chapter does not apply to the following: (a) A lamp used for image capture and projection, including photocopying, printing, directly or in preprocessing, lithography, film and video projection,
• § 109025 — (a) Commencing January 1, 2027, a person or entity shall not manufacture, sell, deliver, distribute, hold, or offer for sale, in commerce a food product for human consumption that contains any of the
• § 109050 — The Legislature finds and declares all of the following: (a) Di(2-ethylhexyl) phthalate (DEHP) and other ortho-phthalates are toxic chemicals and can have negative impacts on human health as determine
• § 109051 — For purposes of this chapter, the following terms have the following definitions: (a) “DEHP” means Di(2-ethylhexyl) phthalate.
• § 109052 — (a) Commencing January 1, 2030, a person or entity shall not manufacture, sell, or distribute into commerce in the State of California intravenous solution containers made with intentionally added DEH
• § 109250 — The effective diagnosis, care, treatment or cure of persons suffering from cancer is of paramount public importance.
• § 109255 — There is in the department a Cancer Advisory Council composed of nine physicians and surgeons licensed to practice medicine in, and residing in, this state, three persons who are not physicians and su
• § 109260 — The members of the council, other than the director of the department, shall receive no compensation for their services, but shall be allowed their actual necessary traveling expenses incurred in the
• § 109265 — The council shall annually elect one of its members to serve as chairman.
• § 109270 — The department shall: (a) Prescribe reasonable regulations with respect to the administration of this article and Article 2 (commencing with Section 109300).
• § 109275 — (a) Upon a diagnosis of breast cancer, the physician and surgeon, meaning the primary provider who initially referred the patient for the screening or biopsy or, if different, the provider who has mad
• § 109276 — In the first revision of the standardized written summary required under subdivision (c) of Section 109275 made following the effective date of the act that added this section, the State Department of
• § 109277 — (a) Every person or entity who owns or operates a health facility or a clinic, or who is licensed as a physician and surgeon and rents or owns the premises where his or her practice is located, shall
• § 109278 — (a) The medical care provider primarily responsible for providing to a patient an annual gynecological examination shall provide to that patient during the annual examination a standardized summary in
• § 109280 — (a) A standardized written summary in layperson’s language and in a language understood by patients shall be approved by the department.
• § 109282 — (a) Every person or entity who owns or operates a health facility or a clinic, or who is licensed as a physician and surgeon and rents or owns the premises where his or her practice is located, shall
• § 109285 — For the purposes of this article and Article 2 (commencing with Section 109300) “cancer” means all malignant neoplasms regardless of the tissue of origin, including malignant lymphoma, Hodgkins diseas
• § 109290 — No person may undertake to treat or alleviate cancer by use of drugs, surgery, or radiation unless the person holds a license issued under a law of this state expressly authorizing the diagnosis and t
• § 109295 — On written request by the department, delivered personally or by mail, any individual, person, firm, association, or other entity engaged, or representing himself, or itself, as engaged, in the diagno
• § 109300 — The sale, offering for sale, holding for sale, delivering, giving away, prescribing or administering of any drug, medicine, compound, or device to be used in the diagnosis, treatment, alleviation, or
• § 109305 — Within 180 days after the filing of an application provided for in subdivision (2) of Section 109300 or an additional period as may be agreed upon by the board and the applicant, the board shall eithe
• § 109310 — In the case of any drug, medicine, compound or device for that an approval of an application filed pursuant to this article and Article 1 (commencing with Section 109250) is in effect, the applicant s
• § 109315 — The board shall issue an order refusing to permit the application to become effective, if, after due notice to the applicant and opportunity for a hearing, the board finds any of the following: (a) Th
• § 109320 — (a) The board shall issue an order withdrawing approval of an application concerning any drug, medicine, compound, or device if, after due notice to the applicant and opportunity for a hearing, the bo
• § 109325 — This article and Article 1 (commencing with Section 109250) shall not apply to the use of any drug, medicine, compound, or device intended solely for legitimate and bona fide investigational purposes
• § 109330 — Section 109300 does not apply to any device used within the scope of his or her license privileges by a physician and surgeon or dentist licensed as such in this state.
• § 109335 — The failure of any individual, person, firm, association, or other entity representing himself, or itself, as engaged in the diagnosis, treatment, alleviation, or cure of cancer to comply with any of
• § 109340 — The investigation or testing of any product shall not be deemed to imply or indicate any endorsement of the qualifications or value of any product.
• § 109345 — Following an investigation or testing of the content or composition of any drug, medicine, compound, or device used by any individual, person, firm, association, or other entity in the diagnosis, trea
• § 109350 — The department may direct that any individual, person, firm, association, or other entity shall cease and desist any further prescribing, recommending, or use of any drug, medicine, compound, or devic
• § 109355 — (a) Any violation of this article and Article 1 (commencing with Section 109250), of the regulations adopted thereunder or of a cease and desist order issued by the department under Section 109345 or
• § 109360 — Any person against whom an injunction or cease and desist order has been issued, under this article and Article 1 (commencing with Section 109250), may not undertake to use in the diagnosis, treatment
• § 109365 — It is unlawful for any person, with the intent to defraud, to falsely represent and provide for compensation a device, substance, method or treatment as effective to diagnose, arrest, prevent, or cure
• § 109370 — Except as provided in Section 109335, a violation of this article and Article 1 (commencing with Section 109250) is punishable by imprisonment in the county jail for a period not exceeding one year, o
• § 109375 — The director shall investigate possible violations of this article and Article 1 (commencing with Section 109250) and report violations to the appropriate enforcement authority.
• § 109380 — County health officers, district attorneys and the Attorney General shall cooperate with the director in the enforcement of this article and Article 1 (commencing with Section 109250).
• § 109385 — The department, upon recommendation of the Cancer Advisory Council, may from time to time publish reports based on its investigation or testing of any drug, medicine, compound, or device prescribed, r
• § 109390 — All hearings authorized by this article and Article 1 (commencing with Section 109250) shall be conducted in accordance with Chapter 5 (commencing with Section 11500) of Part 1, Division 3, Title 2 of
• § 109395 — No provision of this article and Article 1 (commencing with Section 109250) shall preclude reconsideration of an application for use of any drug, medicine, compound or device for the diagnosis, treatm
• § 109500 — As used in this article, “DMSO” means dimethyl sulfoxide.
• § 109505 — DMSO sold in California other than by prescription shall be labeled by the manufacturer, distributor, or seller to contain a description of all of the contents in the solution, statement of purity, th
• § 109525 — This chapter shall be known as the “California Imitation Controlled Substances Act.
• § 109530 — Unless the context otherwise requires, the definitions in this article govern the construction of this chapter.
• § 109535 — “Controlled substance” means a substance as defined in Section 11007.
• § 109540 — “Distribute” means the actual, constructive, or attempted transfer, delivery, or dispensing to another of an imitation controlled substance.
• § 109545 — “Manufacture” means the production, preparation, compounding, processing, encapsulating, packaging or repackaging, labeling or relabeling, of an imitation controlled substance.
• § 109550 — “Imitation controlled substance” means (a) a product specifically designed or manufactured to resemble the physical appearance of a controlled substance, that a reasonable person of ordinary knowledge
• § 109555 — The provisions of this chapter are cumulative, and shall not be construed as restricting any remedy, provisional or otherwise, provided by law for the benefit of any party.
• § 109575 — Any person who knowingly manufactures, distributes, or possesses with intent to distribute, an imitation controlled substance is guilty of a misdemeanor and shall, if convicted, be subject to imprison
• § 109580 — Any person 18 years of age or over who violates Section 109575 by knowingly distributing an imitation controlled substance to a person under 18 years of age is guilty of a misdemeanor and shall, if co
• § 109585 — No civil or criminal liability shall be imposed by virtue of this chapter on any person registered under the California Uniform Controlled Substances Act who manufactures, distributes, or possesses an
• § 109590 — All imitation controlled substances shall be subject to forfeiture in accordance with the procedures set forth in Chapter 8 (commencing with Section 11470) of Division 10.
• § 109875 — This part shall be known as the Sherman Food, Drug, and Cosmetic Law.
• § 109880 — Unless the context otherwise requires, the definitions set forth in this article govern the construction of this part.
• § 109885 — “Advertisement” means any representations, including, but not limited to, statements upon the products, its packages, cartons, and any other container, disseminated in any manner or by any means, for
• § 109890 — “Antibiotic drug” means any drug , except drugs for use in animals other than humans, composed in whole or in part of any form of penicillin, streptomycin, chlortetracycline chloramphenicol, bacitraci
• § 109895 — “Color additive” means a substance that satisfies both of the following requirements: (a) It is a dye, pigment, or other substance made by a process of synthesis or similar artifice, or extracted, iso
• § 109900 — “Cosmetic” means any article, or its components, intended to be rubbed, poured, sprinkled, or sprayed on, introduced into, or otherwise applied to, the human body, or any part of the human body, for c
• § 109905 — “Counterfeit”, as used in respect to any food, drug, device, or cosmetic, means a food, drug, device, or cosmetic that bears or whose package or labeling bears, without authorization, the trademark, t
• § 109910 — “Department” means the State Department of Health Services.
• § 109915 — “Director” means the State Director of Health Services.
• § 109920 — “Device” means any instrument, apparatus, implement, machine, contrivance, implant, in vitro reagent, or other similar or related article, including any component, part, or accessory, that is any of t
• § 109925 — (a) “Drug” means any of the following: (1) An article recognized in an official compendium.
• § 109930 — “Federal act” means the federal Food, Drug, and Cosmetic Act, as amended (21 U.
• § 109935 — “Food” means either of the following: (a) Any article used or intended for use for food, drink, confection, condiment, or chewing gum by man or other animal.
• § 109940 — “Food additive” means any substance, the intended use of which results or may reasonably be expected to result, directly or indirectly, in the substance becoming a component of the food or otherwise a
• § 109945 — “Food and drug inspector” means any authorized agent of the Bureau of Food and Drug of the department, who shall have the powers set forth in Section 106500.
• § 109947 — “Food processing facility” means any facility operated for the purposes of manufacturing, packing, or holding processed food.
• § 109948 — (a) “Home medical device retail facility” is an area, place, or premises, other than a licensed pharmacy, in and from which prescription devices, home medical devices, or home medical device services
• § 109948.1 — (a) “Home medical device services” means the delivery, installation, maintenance, replacement of, or instruction in the use of, home medical devices used by a sick or disabled individual to allow the
• § 109950 — “Immediate container” does not include any package liner.
• § 109951 — “Infant formula” shall have the same definition as that term is used in the Federal Food, Drug, and Cosmetic Act (21 U.
• § 109955 — “Label” means a display of written, printed, or graphic matter upon a food, drug, device, or cosmetic or upon its immediate container.
• § 109960 — “Labeling” means any label or other written, printed, or graphic matter upon a food, drug, device, or cosmetic or upon its container or wrapper, or that accompanies any food, drug, device, or cosmetic
• § 109965 — “Local health department” means the health department of a city, county, city and county, or local health district that qualifies for state assistance pursuant to Chapter 3 (commencing with Section 10
• § 109970 — “Manufacture” means the preparation, compounding, propagation, processing, or fabrication of any food, drug, device, or cosmetic.
• § 109971 — “Medical food” means any product that meets the definition of medical food in the Federal Food, Drug, and Cosmetic Act (21 U.
• § 109975 — “New device” means any of the following: (a) Any device the composition, construction, or properties of which are such that the device is not generally recognized, among experts qualified by scientifi
• § 109980 — “New drug” means either of the following: (a) Any drug the composition of which is such that the drug is not generally recognized, among experts qualified by scientific training and experience to eval
• § 109985 — “Official compendium” means the latest edition of the United States Pharmacopoeia, the latest edition of the Homeopathic Pharmacopoeia of the United States, or the latest edition of the National Formu
• § 109990 — “Package” means any container or wrapper that may be used by a manufacturer, producer, jobber, packer, or dealer for enclosing or containing any food, drug, device, or cosmetic.
• § 109992 — “Pasteurized in-shell eggs” means shell eggs that have been pasteurized by any method approved by the federal Food and Drug Administration, the Department of Food and Agriculture, or the department.
• § 109995 — “Person” means any individual, firm, partnership, trust, corporation, limited liability company, company, estate, public or private institution, association, organization, group, city, county, city an
• § 11 — The present tense includes the past and future tenses; and the future, the present.
• § 11000 — This division shall be known as the “California Uniform Controlled Substances Act.
• § 110000 — “Pesticide chemical” means any substance that alone, in chemical combination, or in formulation with one or more substances, is an “economic poison” within the meaning of Section 12753 of the Food and
• § 110005 — “Potentially hazardous food” means any food capable of supporting growth of infectious or toxigenic micro-organisms when held at temperatures above 45 degrees Fahrenheit.
• § 11001 — Unless the context otherwise requires, the definitions in this chapter govern the construction of this division.
• § 110010 — “Prescription” means an oral order given individually for the patient for whom prescribed directly from the prescriber to the furnisher or indirectly by means of a written order signed by the prescrib
• § 110010.1 — “Prescription device” means any device limited to prescription use under Section 111470.
• § 110010.2 — “Prescription drug” means any drug limited to prescription use under Section 111470.
• § 110015 — “Principal display panel” means that part of a label most likely to be displayed, presented, shown, or examined under normal and customary conditions of display for retail sale.
• § 11002 — “Administer” means the direct application of a controlled substance, whether by injection, inhalation, ingestion, or any other means, to the body of a patient for his immediate needs or to the body of
• § 110020 — “Raw agricultural commodity” means any food in its raw or natural state.
• § 110025 — (a) “Substantial evidence” means evidence consisting of adequate and well-controlled investigations, including clinical investigations, by experts qualified by scientific training and experience to ev
• § 11003 — “Agent” means an authorized person who acts on behalf of or at the direction of a manufacturer, distributor, or dispenser.
• § 110030 — The provisions of this part regarding the selling of any food, drug, device, or cosmetic include, but are not limited to, all of the following: (a) The manufacture, production, processing, and packing
• § 110035 — All regulations pertaining to any food, drug, device, or cosmetic adopted by the department that are in effect on the effective date of this part shall remain in effect until the department adopts reg
• § 110036 — All laws and regulations pertaining to industrial hemp products shall remain in effect until the adoption of regulations pursuant to the federal law that authorizes industrial hemp products.
• § 11004 — “Attorney General” means the Attorney General of the State of California.
• § 110040 — This part shall be so construed as to not be in conflict with the Food and Agricultural Code, or with the Alcoholic Beverage Control Act, Division 9 (commencing with Section 23000) of the Business and
• § 110045 — The department shall administer and enforce this part.
• § 11005 — “Board of Pharmacy” means the California State Board of Pharmacy.
• § 110050 — The Food Safety Fund is hereby created as a special fund in the State Treasury.
• § 110055 — All money collected by the department under Sections 111830, 111885, and 111905 shall be deposited into the State Treasury to the credit of the General Fund.
• § 11006.5 — (a) Before January 1, 2026, “concentrated cannabis” means the separated resin, whether crude or purified, obtained from cannabis.
• § 110060 — The director and authorized agents of the department shall have the powers set forth in Sections 100165 and 106500.
• § 110061 — For the purposes of administering this part, Part 6 (commencing with Section 111940) of Division 104 of the Health and Safety Code, Section 104559.
• § 110065 — (a) The department may adopt any regulations that it determines are necessary for the enforcement of this part.
• § 11007 — “Controlled substance,” unless otherwise specified, means a drug, substance, or immediate precursor which is listed in any schedule in Section 11054, 11055, 11056, 11057, or 11058.
• § 110070 — Whenever public health or other considerations in this state require, the department may adopt, upon its own motion, or upon the petition of any interested party, regulations that prescribe tolerances
• § 110075 — In adopting regulations, pursuant to Section 110070 of this part, the department shall consider all of the following factors that the petitioner shall furnish: (a) The name and all pertinent informati
• § 11008 — “Customs broker” means a person in this state who is authorized to act as a broker for any of the following: (a) A person in this state who is licensed to sell, distribute, or otherwise possess any co
• § 110080 — (a) All pesticide regulations and any amendments to these regulations adopted pursuant to the federal act or the Food and Agricultural Code, in effect on November 23, 1970, or adopted on or after this
• § 110085 — All food additive regulations and any amendments to the regulations adopted pursuant to the federal act in effect on November 23, 1970, or adopted on or after that date, are the food additive regulati
• § 11009 — “Deliver” or “delivery” means the actual, constructive, or attempted transfer from one person to another of a controlled substance, whether or not there is an agency relationship.
• § 110090 — All color additive regulations and any amendments to the regulations adopted pursuant to the federal act, in effect on November 23, 1970, or adopted on or after that date, are the color additive regul
• § 110095 — All special dietary use regulations and any amendments to regulations adopted pursuant to the federal act, in effect on November 23, 1970, or adopted on or after that date, are the special dietary use
• § 11010 — “Dispense” means to deliver a controlled substance to an ultimate user or research subject by or pursuant to the lawful order of a practitioner, including the prescribing, furnishing, packaging, label
• § 110100 — (a) All food labeling regulations and any amendments to those regulations adopted pursuant to the federal act, in effect on January 1, 1993, or adopted on or after that date shall be the food labeling
• § 110105 — All good manufacturing practices regulations for any food, drug, device, or cosmetic and any amendments to the regulations adopted pursuant to the federal act in effect on November 23, 1970, or adopte
• § 11011 — “Dispenser” means a practitioner who dispenses.
• § 110110 — (a) All regulations relating to (1) new drug applications, except for abbreviated new drug applications, adopted pursuant to Section 505 of the federal act (21 U.
• § 110111 — All nonprescription drug regulations and any amendments to those regulations adopted pursuant to the federal act, that are in effect on January 1, 2000, or that are adopted on or after that date, shal
• § 110115 — A federal regulation adopted pursuant to this part takes effect in this state 30 days after it becomes effective as a federal regulation.
• § 11012 — “Distribute” means to deliver other than by administering or dispensing a controlled substance.
• § 110120 — If no substantial objections are received and no hearing is requested within 30 days after publication of a newly proposed state regulation, it shall take effect on the date set by the department.
• § 110125 — If substantial objections are made to a federal regulation within 30 days prior to its becoming effective in this state or to a proposed regulation within 30 days after it is published, the department
• § 11013 — “Distributor” means a person who distributes.
• § 110130 — Hearings authorized or required by this part shall be conducted by the department or agent as the department may designate for that purpose.
• § 110135 — Before any alleged violation of this part is reported to the Attorney General, a district attorney, or a city attorney for the institution of a criminal proceeding, the person against whom this procee
• § 11014 — “Drug” means (a) substances recognized as drugs in the official United States Pharmacopoeia, official Homeopathic Pharmacopoeia of the United States, or official National Formulary, or any supplement
• § 11014.5 — (a) “Drug paraphernalia” means all equipment, products, and materials of any kind that are designed for use or marketed for use, in planting, propagating, cultivating, growing, harvesting, manufacturi
• § 110140 — For purposes of enforcement of this part, any authorized agent of the department may, upon presenting appropriate credentials and at a reasonable time, do any of the following: (a) Enter any factory,
• § 110145 — The inspection authorized by Section 110140 shall not include any of the following: (a) Financial data.
• § 11015 — “Federal bureau” means the Drug Enforcement Administration of the United States Department of Justice, or its successor agency.
• § 110150 — An authorized agent of the department may secure any sample or specimen of any food, drug, device, or cosmetic.
• § 110155 — An authorized agent of the department shall have access to all records of carriers in commerce relating to the movement in commerce of any food, drug, device, or cosmetic, or the holding of that food,
• § 11016 — “Furnish” has the same meaning as provided in Section 4048.
• § 110160 — It is unlawful for any person to refuse to permit entry or inspection, the taking of samples or other evidence, or access to copying of any record as authorized by this part, or to conceal the samples
• § 110165 — It is unlawful for any person to use to his or her own advantage, or to reveal to any person other than to the director, officers, employees, or authorized agents of this department, or to the courts
• § 11017 — “Manufacturer” has the same meaning as provided in Section 4034 of the Business and Professions Code.
• § 110170 — The department may publish reports summarizing all judgments and court orders that have been rendered under this part, including the nature of the charge and the disposition of the charge.
• § 110175 — The department may distribute information regarding any food, drug, device, or cosmetic as the department considers necessary for the protection of the health and safety of the consumer or for his or
• § 11018 — “Cannabis” means all parts of the plant Cannabis sativa Linnaeus, Cannabis indica, or Cannabis ruderalis, whether growing or not; the seeds thereof; the resin from glandular trichomes or extracted fro
• § 11018.1 — (a) “Cannabis products” means a product containing cannabis or cannabis concentrate and includes, but is not limited to, edible, topical, and inhaled products, and products intended for use on, or con
• § 11018.2 — “Cannabis accessories” means any equipment, products or materials of any kind which are used, intended for use, or designed for use in planting, propagating, cultivating, growing, harvesting, manufact
• § 11018.5 — (a) (1) “Industrial hemp” or “hemp” means types of the plant Cannabis sativa Linnaeus or any part of that plant with a total tetrahydrocannabinol concentration of no more than 0.
• § 110180 — The department may collect, report, or illustrate the results of any investigation of the department.
• § 11019 — “Narcotic drug” means any of the following, whether produced directly or indirectly by extraction from substances of vegetable origin, or independently by means of chemical synthesis, or by a combinat
• § 110190 — (a) Any person who ships to another state or country a food, drug, device, or cosmetic manufactured or produced in this state may request the department to issue an export document to reference the sh
• § 11020 — “Opiate” means any substance having an addiction-forming or addiction-sustaining liability similar to morphine or being capable of conversion into a drug having addiction-forming or addiction-sustaini
• § 110200 — (a) Each export document issued by the department shall do all of the following: (1) Identify either or both of the following: (A) The name and place of business of the manufacturer or producer of the
• § 11021 — “Opium poppy” means the plant of the species Papaver somniferum L.
• § 110210 — (a) Each person requesting the department to issue an export document shall pay nonreturnable fees as follows: (1) A one-time fee of one hundred dollars ($100).
• § 11022 — “Person” means individual, corporation, government or governmental subdivision or agency, business trust, estate, trust, partnership, limited liability company, or association, or any other legal enti
• § 110220 — (a) The department may refuse to accept any request where the information required to be submitted by this article is incomplete.
• § 110225 — It is unlawful for any person to knowingly supply the department with false material facts in a request for an export document or to falsely represent that the department has issued an export document
• § 11023 — “Pharmacy” has the same meaning as provided in Section 4035 of the Business and Professions Code.
• § 110230 — Any person who has a valid registration, license, certificate, or permit issued by the department to manufacture or produce a food, drug, device, or cosmetic in this state may request the department t
• § 110235 — (a) Each person requesting the department to issue an official copy of a valid registration, license, certificate, or permit shall pay nonreturnable fees as follows: (1) Fifteen dollars ($15) per offi
• § 11024 — “Physician,” “dentist,” “podiatrist,” “pharmacist,” “veterinarian,” and “optometrist” means persons who are licensed to practice their respective professions in this state.
• § 110240 — There is established an Export Document Program Fund within the General Fund.
• § 110241 — All fees collected by the department pursuant to requests to conduct a voluntary medical device review shall be deposited into the Export Document Program Fund and, upon appropriation, shall be expend
• § 110242 — (a) The California Rx Prescription Drug Web Site Program is hereby established.
• § 110243 — (a) Contracts and change orders entered into pursuant to this article and any project or systems development notice shall be exempt from all of the following: (1) The competitive bidding requirements
• § 110245 — No dealer shall be prosecuted under this part for a violation concerning any food, drug, device, or cosmetic that is contained in an original, unbroken, and undamaged package that bears the original l
• § 11025 — “Poppy straw” means all parts, except the seeds, of the opium poppy, after mowing.
• § 110250 — The guarantee shall be dated prior to the date of sale of the food, drug, device, or cosmetic and it shall be signed by the wholesaler, jobber, manufacturer, or other person located or residing in thi
• § 110255 — A guarantee may be either a general guarantee or a special guarantee and shall be produced prior to the time of reporting an alleged violation to the Attorney General, the district attorney, or a city
• § 11026 — “Practitioner” means any of the following: (a) A physician, dentist, veterinarian, podiatrist, or pharmacist acting within the scope of a project authorized under Article 1 (commencing with Section 12
• § 110260 — A general guarantee shall guarantee without condition or restriction any food, drug, device, or cosmetic that is produced, prepared, compounded, packed, distributed, or sold by the guarantor as not ad
• § 110265 — A special guarantee shall guarantee in the same manner as a general guarantee the particular food, drug, device, or cosmetic listed in an invoice of the food, drug, device, or cosmetic, and shall be a
• § 11027 — (a) “Prescription” means an oral order or electronic transmission prescription for a controlled substance given individually for the person(s) for whom prescribed, directly from the prescriber to the
• § 110270 — All guarantees shall contain the name and address of the guarantor making the sale of food, drug, device, or cosmetic.
• § 110275 — It is unlawful for any person to give a guarantee or undertaking that is false.
• § 110280 — If the guarantee is to the effect that the food, drug, device, or cosmetic is not in violation within the meaning of the federal act, it shall be sufficient for all the purposes of this part, and shal
• § 110285 — In any case where the department has adopted a regulation prescribing a tolerance, including, but not limited to, a zero tolerance, for a poisonous or deleterious substance, food additive, pesticide c
• § 110286 — (a) A retailer shall not sell or offer for sale after the expiration date an over-the-counter drug.
• § 11029 — “Production” includes the manufacture, planting, cultivation, growing, or harvesting of a controlled substance.
• § 11029.5 — “Security printer” means a person approved to produce controlled substance prescription forms pursuant to Section 11161.
• § 110290 — In determining whether the labeling or advertisement of a food, drug, device, or cosmetic is misleading, all representations made or suggested by statement, word, design, device, sound, or any combina
• § 110295 — The requirement that any word, statement, or other information appear on the label shall not be considered to be complied with unless the word, statement, or other information also appears on the outs
• § 11030 — “Ultimate user” means a person who lawfully possesses a controlled substance for his own use or for the use of a member of his household or for administering to an animal owned by him or by a member o
• § 110300 — It is unlawful for any person to forge, counterfeit, simulate, falsely represent, or without proper authority use, any mark, stamp, tag, label, or other identification device that is authorized or req
• § 11031 — “Wholesaler” has the same meaning as provided in Section 4038 of the Business and Professions Code.
• § 110310 — It is unlawful for any manufacturer, packer, or distributor of a prescription drug or device offered for sale in this state to fail to maintain for transmittal or to fail to transmit to any practition
• § 110315 — It is unlawful for any person, with the intent to deceive, to place, or cause to be placed upon any food, drug, device, or cosmetic, or its package, the trade name or other identifying mark or imprint
• § 11032 — If reference is made to the term “narcotics” in any law not in this division, unless otherwise expressly provided, it means those controlled substances classified in Schedules I and II, as defined in
• § 110320 — It is unlawful for any person to sell, dispense, dispose of, hold, or conceal any food, drug, device, or cosmetic or its package, with knowledge that the trade name or other identifying marks, imprint