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Nonprescription Drug Product With an Additional Condition for Nonprescription Use

other · Food and Drug Administration · Rule · Published 2024-12-26 · Effective 2025-01-27 · 89 FR 105288

Document

Document number
2024-30261
Federal Register citation
89 FR 105288
CFR reference
21 CFR 201
Type
Rule
Action
Final rule.
Category
other
Sub-agency
Food and Drug Administration
Publication date
2024-12-26
Effective date
2025-01-27
HHS docket
Docket No. FDA-2021-N-0862

Abstract

The Food and Drug Administration (FDA, the Agency, or we) is issuing a final rule to establish requirements for a nonprescription drug product with an additional condition for nonprescription use (ACNU). A nonprescription drug product with an ACNU is a drug product that could be marketed without a prescription if an applicant implements an additional condition to ensure appropriate self-selection or appropriate actual use, or both, by consumers without the supervision of a practitioner licensed by law to administer such drug. The final rule is intended to increase options for applicants to develop and market safe and effective nonprescription drug products and increase consumer access to appropriate, safe, and effective drug products, which could improve public health.

Source

Authoritative
Federal Register document
Machine
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