Title 21. Food, Drugs, and Cosmetics — Subtitle 11. Miscellaneous Drug and Cosmetic Provisions
Statutes in effect as of October 1, 2026.
Md. Code Ann., Health-Gen. § 21-1110 (2026)
Title 21. Food, Drugs, and Cosmetics
Subtitle 11. Miscellaneous Drug and Cosmetic Provisions
§ 21–1110LinkCopy Citation
(a)
This section does not apply to cosmetics, infant formula, or baby food if:
(1)
The cosmetics, infant formula, or baby food are being sold in a single lot at a charity auction; and
(2)
The total value of the cosmetics, infant formula, or baby food in the lot is $100 or less.
(b)
A person may not sell any drug, medicine, cosmetic, pharmaceutical preparation, medicinal preparation, or infant formula or baby food that is subject to dating requirements by the United States Food and Drug Administration at any auction sale unless the person notifies the Secretary in writing of the proposed auction at least 7 days before the date of the auction.
(c)
(1)
The Secretary may:
(i)
Inspect any drugs, medicines, cosmetics, pharmaceutical preparations, medicinal preparations, infant formula, or baby food that a person proposes to sell by auction sale; and
(ii)
Issue an order that prohibits the sale of any of these if, in the opinion of the Secretary, they are unfit for human use or consumption.
(2)
A person may not hold an auction sale of any drug, medicine, cosmetic, pharmaceutical preparation, medicinal preparation, infant formula, or baby food in violation of an order issued under this section.
Md. Code Ann., Health-Gen. § 21-1111 (2026)
Title 21. Food, Drugs, and Cosmetics
Subtitle 11. Miscellaneous Drug and Cosmetic Provisions
§ 21–1111LinkCopy Citation
(a)
This section does not apply to any:
(1)
Surgical or dental instrument;
(2)
Physical therapy equipment;
(3)
X–ray apparatus; or
(4)
Component part or accessory of any of these items.
(b)
A person may not:
(1)
Sell, distribute, or otherwise dispose of any drug, medicine, pharmaceutical preparation, or medicinal preparation by means of any public exhibition, entertainment, performance, or carnival, commonly known as a “medicine show” or “patent medicine show”; or
(2)
Put or cause to be put, in any way, any package, parcel, or sample of any drug or medicine:
(i)
In or on any part of any house, building, or yard without the consent of the owner or occupant; or
(ii)
On any street or public highway.
Md. Code Ann., Health-Gen. § 21-1112 (2026)
Title 21. Food, Drugs, and Cosmetics
Subtitle 11. Miscellaneous Drug and Cosmetic Provisions
§ 21–1112LinkCopy Citation
(a)
(1)
In this section the following terms have the meanings indicated.
(2)
“Authorized prescriber” means a licensed dentist, licensed physician, licensed podiatrist, licensed veterinarian, certified nurse midwife to the extent permitted under § 8–601 of the Health Occupations Article, certified nurse practitioner to the extent permitted under § 8–508 of the Health Occupations Article, or other individual authorized by law to prescribe prescription or nonprescription drugs or devices.
(3)
“Board” means a health occupation licensing board authorized to issue a permit, license, or certificate under the Health Occupations Article.
(4)
(i)
“Controlled dangerous substance” means a drug, substance, or immediate precursor listed in Schedule I through Schedule V in Title 5 of the Criminal Law Article.
(ii)
“Controlled dangerous substance” does not include tobacco or a distilled spirit, wine, or malt beverage.
(5)
“Drug” means a prescription or nonprescription drug.
(6)
“Nonprescription drug” means a drug which may be sold without a prescription and which is labeled for consumer use in accordance with the requirements of the laws and regulations of this State and the federal government.
(7)
“Permit holder” means a holder of, or applicant for:
(i)
A pharmacy permit or distributor’s permit issued by the State Board of Pharmacy under Title 12 of the Health Occupations Article;
(ii)
A dispensing permit issued by a board under the authority of § 12–102(c)(2) of the Health Occupations Article; or
(iii)
A controlled dangerous substances registration issued by the Office of Controlled Substances Administration under § 5–301(a)(1) of the Criminal Law Article.
(8)
“Prescription drug” means a drug that under § 21–220 of this title may be dispensed only on the prescription of a health practitioner who is authorized by law to prescribe the drug.
(b)
(1)
The Department may issue an order of impoundment and immediately impound drugs, bulk powders and chemicals, or prescription records of a permit holder or an authorized prescriber if:
(i)
A permit holder’s permit or authorized prescriber’s license has expired or has been revoked or suspended;
(ii)
An application for a permit or license has been denied;
(iii)
A board has:
(1)
Determined that the permit holder or authorized prescriber failed to comply with a board order, letter of surrender, or law regarding the disposition of drugs, bulk powders and chemicals, or prescription records; and
(2)
Requested that the Department impound the drugs, bulk powders and chemicals, or prescription records;
(iv)
The drugs or bulk powders and chemicals pose an imminent threat to the public health, safety, or welfare; or
(v)
The confidentiality of the prescription records is in imminent danger of being compromised.
(2)
The Department may not impound the drugs, bulk powders and chemicals, or prescription records of a permit holder or authorized prescriber who is in compliance with a board order or law specifically providing for the manner of the disposition of drugs, bulk powders and chemicals, or prescription records.
(c)
(1)
Except as otherwise provided in paragraph (2) of this subsection, the Department shall:
(i)
Attempt to serve written notice of an impoundment on the permit holder or authorized prescriber;
(ii)
Provide the permit holder or authorized prescriber with an opportunity to avoid impoundment by allowing the permit holder or authorized prescriber to dispose of the drugs, bulk powders and chemicals, or prescription records in a manner acceptable to the Department;
(iii)
Provide the permit holder or authorized prescriber with an opportunity prior to impoundment to review the nature, type, and amount of information upon which the Department issued the impoundment order; and
(iv)
Provide the permit holder or authorized prescriber with an opportunity to avoid impoundment by providing the Department with information upon which the Department could reasonably conclude that the impoundment is not warranted.
(2)
If drugs or bulk powders and chemicals pose an imminent threat to the public health, safety, or welfare, or if the confidentiality of prescription records is in imminent danger of being compromised, the Department may:
(i)
Issue an impoundment order; and
(ii)
Immediately impound drugs, bulk powders and chemicals, or prescription records without prior notice to the permit holder or authorized prescriber.
(d)
An order of impoundment constitutes a final order subject to judicial review under the State Administrative Procedure Act.
(e)
The Department shall provide the permit holder or authorized prescriber with a list of all drugs, bulk powders and chemicals, and prescription records impounded.
(f)
The Department may charge reasonable fees to recover the costs of the collection, storage, and disposition of drugs, bulk powders and chemicals, or prescription records.
(g)
The Department shall adopt regulations governing the disposition of impounded drugs, bulk powders and chemicals, and prescription records.
(h)
Prior to issuing an order of impoundment, the Department, with the approval of the Board of Pharmacy, shall develop regulations concerning:
(1)
The nature, type, and amount of information upon which the Department may rely to issue an order of impoundment;
(2)
The level of investigation the Department must pursue to verify the information upon which the order of impoundment was based under subsection (b)(1)(iv) or (v) or (c)(2) of this section; and
(3)
The measures the Department must pursue to attempt service on the permit holder or authorized prescriber prior to impoundment under subsection (c) of this section.
(i)
Prior to destroying or transferring impounded drugs, bulk powders and chemicals, or prescription records, the Department shall publish a notice once a week for 2 consecutive weeks in a newspaper that is circulated locally:
(1)
Stating the date that the drugs, bulk powders and chemicals, or prescription records will be destroyed or transferred; and
(2)
Designating a date, time, and location where the drugs, bulk powders and chemicals, or prescription records may be retrieved by the permit holder or authorized prescriber if certain conditions are met.
(j)
A board shall immediately notify the Office of Controlled Substances Administration of the surrender, suspension, or revocation of a permit holder’s permit or an authorized prescriber’s license.
Md. Code Ann., Health-Gen. § 21-1113 (2026)
Title 21. Food, Drugs, and Cosmetics
Subtitle 11. Miscellaneous Drug and Cosmetic Provisions
§ 21–1113LinkCopy Citation
In any action brought by the Attorney General under § 11–209 of the Commercial Law Article, a person that sells, distributes, or otherwise disposes of any drug, medicine, cosmetic, food, food additive, or commercial feed, as defined in § 6–101 of the Agriculture Article, or medical device:
(1)
May not assert as a defense that the person did not deal directly with the person on whose behalf the action is brought; and
(2)
May prove, as a partial or complete defense against a damage claim, in order to avoid duplicative liability, that all or any part of an alleged overcharge ultimately was passed on to another person by a purchaser or seller in the chain of manufacture, production, or distribution who paid the alleged overcharge.