Code of Virginia
Chapter 34 - Drug Control Act
§ 54.1-3465. Misbranded cosmetics

A cosmetic shall be deemed to be misbranded:
1. If its labeling is false or misleading in any particular;
2. If in package form unless it bears a label containing the name and place of business of the manufacturer, packer, or distributor and an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count. However, reasonable variations shall be permitted, and exemptions for small packages shall be established by the Board;
3. If any word, statement, or other information required by or under authority of this chapter to appear on the label or 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 its container is so made, formed or filled as to be misleading;
5. If it is a color additive, unless its packaging and labeling are in conformity with packaging and labeling requirements applicable to such color additive under the provisions of the federal act. This subdivision shall not apply to packages of color additives which, with respect to their use for cosmetics, are marketed and intended for use only in or on hair dyes.
A cosmetic which is, in accordance with the practice of the trade, to be processed, labeled or repacked in substantial quantities at an establishment other than the establishment where it was originally processed or packed, is exempted from the affirmative labeling requirements of this chapter while it is in transit in commerce from the one establishment to the other, if such transit is made in good faith for such completion purposes only; but it is otherwise subject to all applicable provisions of this chapter.
Code 1950, § 54-466; 1970, c. 650, § 54-524.97; 1988, c. 765.

Structure Code of Virginia

Code of Virginia

Title 54.1 - Professions and Occupations

Chapter 34 - Drug Control Act

§ 54.1-3400. Citation

§ 54.1-3401. Definitions

§ 54.1-3401.1. Repealed

§ 54.1-3402. Repealed

§ 54.1-3403. Chapter not applicable to economic poisons

§ 54.1-3404. Inventories of controlled substances required of certain persons; contents and form of record

§ 54.1-3405. Access to and copies of records; inspections

§ 54.1-3406. Records confidential; disclosure of information about violations of federal law

§ 54.1-3407. Analysis of controlled substances

§ 54.1-3408. Professional use by practitioners

§ 54.1-3408.01. Requirements for prescriptions

§ 54.1-3408.02. Transmission of prescriptions

§ 54.1-3408.03. Dispensing of therapeutically equivalent drug product permitted

§ 54.1-3408.04. Dispensing of interchangeable biosimilars permitted

§ 54.1-3408.05. Use of FDA-approved substance upon publication of final rule

§ 54.1-3408.1. Prescription in excess of recommended dosage in certain cases

§ 54.1-3408.2. Failure to report administration or dispensing of or prescription for controlled substances; report required; penalty

§ 54.1-3408.3. Certification for use of cannabis oil for treatment

§ 54.1-3408.4. Expired

§ 54.1-3408.5. Epinephrine required in certain public places

§ 54.1-3409. Professional use by veterinarians

§ 54.1-3410. When pharmacist may sell and dispense drugs

§ 54.1-3410.1. Requirements for radiopharmaceuticals

§ 54.1-3410.2. Compounding; pharmacists' authority to compound under certain conditions; labeling and record maintenance requirements

§ 54.1-3411. When prescriptions may be refilled

§ 54.1-3411.1. Prohibition on returns, exchanges, or re-dispensing of drugs; exceptions

§ 54.1-3411.2. Prescription drug disposal programs

§ 54.1-3411.2:1. Guidelines for disposal of unused drugs

§ 54.1-3412. Date of dispensing; initials of pharmacist; automated data processing system

§ 54.1-3413. Manufacturing and administering Schedule I drugs

§ 54.1-3414. Official orders for Schedule II drugs

§ 54.1-3415. Distribution of drugs in Schedules II through VI by manufacturers and wholesalers

§ 54.1-3415.1. Delivery of medical devices on behalf of a medical equipment supplier

§ 54.1-3416. No prescription for preparations listed pursuant to Schedule V

§ 54.1-3417. Disposing of stocks of Schedules II through V drugs

§ 54.1-3418. Sale of aqueous or oleaginous solutions

§ 54.1-3419. Dispensing of insulin preparations

§ 54.1-3420. Distribution of certain drugs; written request or confirmation of receipt

§ 54.1-3420.1. Identification required for filling prescriptions

§ 54.1-3420.2. Delivery of prescription drug order

§ 54.1-3421. New drugs

§ 54.1-3422. Controlled substances registration certificate required in addition to other requirements; exemptions

§ 54.1-3423. Board to issue registration unless inconsistent with public interest; authorization to conduct research; application and fees

§ 54.1-3424. Suspension or revocation of registration, license or permit; limitation to particular controlled substance; controlled substances placed under seal; sale of perishables and forfeiture; notification to DEA

§ 54.1-3425. Repealed

§ 54.1-3426. Regulations for special packaging

§ 54.1-3427. Dispensing drugs without safety closure container

§ 54.1-3428. Dissemination of information

§ 54.1-3429. Revocation of permit issued to manufacturer, wholesaler or distributor

§ 54.1-3430. Display of permit; permits nontransferable; renewal

§ 54.1-3431. Admission into evidence of certain certificates of analysis

§ 54.1-3432. Supervision by pharmacist

§ 54.1-3433. Certain advertising and signs unlawful

§ 54.1-3434. Permit to conduct pharmacy

§ 54.1-3434.01. Notice of pharmacy closing; change of ownership; penalty

§ 54.1-3434.02. Automated drug dispensing systems

§ 54.1-3434.03. Continuous quality improvement program

§ 54.1-3434.04. Automatic review of certain case decisions

§ 54.1-3434.05. Permit to act as an outsourcing facility

§ 54.1-3434.1. Nonresident pharmacies to register with Board

§ 54.1-3434.2. Permit to be issued

§ 54.1-3434.3. Denial, revocation, suspension of registration, summary proceedings

§ 54.1-3434.4. Prohibited acts

§ 54.1-3434.5. Nonresident outsourcing facilities to register with the Board

§ 54.1-3435. License to act as wholesale distributor; renewal; fee

§ 54.1-3435.01. Registration of nonresident wholesale distributors; renewal; fee

§ 54.1-3435.02. Certain permitted pharmacies and medical equipment suppliers exempted

§ 54.1-3435.1. Denial, revocation, and suspension of license, permit, or registration of certain entities

§ 54.1-3435.2. Permit to act as medical equipment supplier; storage; limitation; regulations

§ 54.1-3435.3. Inspection and audit

§ 54.1-3435.3:1. Registration of nonresident medical equipment suppliers; renewal; fee

§ 54.1-3435.4. Permit to act as warehouser; regulations

§ 54.1-3435.4:01. Registration to act as a nonresident warehouser; regulations

§ 54.1-3435.4:1. Permitting of third-party logistics provider; renewal

§ 54.1-3435.4:2. Registration of nonresident third-party logistics provider; renewal

§ 54.1-3435.5. Repealed

§ 54.1-3436. Repealed

§ 54.1-3436.1. Prescription drug price transparency

§ 54.1-3437. Permit to manufacture drugs

§ 54.1-3437.1. Limited permit for repackaging drugs

§ 54.1-3438. Manufacturing, etc., of drugs or proprietary medicines, to be supervised by pharmacist

§ 54.1-3439. Application for nonrestricted manufacturing permit; fee

§ 54.1-3440. Persons to whom nonrestricted permit is granted

§ 54.1-3441. Restricted manufacturing permit; application; fee; separate application and permit for each place of manufacturing

§ 54.1-3442. When permit not to be granted; regulations

§ 54.1-3442.01. Registration of nonresident manufacturer; renewal

§ 54.1-3442.02. Prescription drug price transparency

§ 54.1-3442.1. Definitions

§ 54.1-3442.2. Eligibility for expanded access to investigational drugs, biological products, and devices; written, informed consent to treatment

§ 54.1-3442.3. Expanded access to investigational drugs, biological products, or devices; cost; insurance coverage

§ 54.1-3442.4. Limitation of liability

§ 54.1-3442.5. Definitions

§ 54.1-3442.6. Permit to operate pharmaceutical processor or cannabis dispensing facility

§ 54.1-3442.7. Dispensing cannabis products; report

§ 54.1-3442.8. Criminal liability; exceptions

§ 54.1-3443. Board to administer article

§ 54.1-3444. Controlled substances included by whatever name designated

§ 54.1-3445. Placement of substance in Schedule I

§ 54.1-3446. Schedule I

§ 54.1-3447. Placement of substance in Schedule II

§ 54.1-3448. Schedule II

§ 54.1-3449. Placement of substance in Schedule III

§ 54.1-3450. Schedule III

§ 54.1-3451. Placement of substance in Schedule IV

§ 54.1-3452. Schedule IV

§ 54.1-3453. Placement of substance in Schedule V

§ 54.1-3454. Schedule V

§ 54.1-3455. Schedule VI

§ 54.1-3456. Controlled substance analog

§ 54.1-3456.1. Drugs of concern

§ 54.1-3457. Prohibited acts

§ 54.1-3458. Violations

§ 54.1-3459. Tagging of adulterated or misbranded drugs, devices, or cosmetics; condemnation; destruction; expenses

§ 54.1-3460. Poisonous or deleterious substance, or color additive

§ 54.1-3461. Adulterated drug or device

§ 54.1-3462. Misbranded drug or device

§ 54.1-3463. Exemption of drugs dispensed by filling or refilling prescription

§ 54.1-3464. Adulterated cosmetics

§ 54.1-3465. Misbranded cosmetics

§ 54.1-3466. Possession or distribution of controlled paraphernalia; definition of controlled paraphernalia; evidence; exceptions

§ 54.1-3467. Distribution of hypodermic needles or syringes, gelatin capsules, quinine or any of its salts

§ 54.1-3468. Conditions to dispensing device, item, or substance; records

§ 54.1-3469. Storage, usage, and disposition of controlled paraphernalia

§ 54.1-3470. Obtaining controlled paraphernalia by fraud, etc.

§ 54.1-3471. Issuance of permits to certain persons other than registered pharmacists

§ 54.1-3472. Article inapplicable to certain persons