# Use of Ozone-Depleting Substances
> **Food and Drug Administration** · Direct final rule. · Published 2016-10-26 · Effective 2017-02-23 · 81 FR 74298
## Document
- **Document number:** 2016-25851
- **Category:** other
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 81 FR 74298
- **CFR reference:** 21 CFR 2
- **Publication date:** 2016-10-26
- **Effective date:** 2017-02-23
- **HHS docket:** Docket No. FDA-2015-N-1355
## Abstract

The Food and Drug Administration (FDA, the Agency, or we) is amending its regulation on uses of ozone-depleting substances (ODSs), including chlorofluorocarbons (CFCs), to remove the designation for certain products as "essential uses" under the Clean Air Act. Essential-use products are exempt from the ban by FDA on the use of CFCs and other ODS propellants in FDA-regulated products and from the ban by the Environmental Protection Agency (EPA) on the use of ODSs in pressurized dispensers. The products that will no longer constitute an essential use are: Sterile aerosol talc administered intrapleurally by thoracoscopy for human use and metered-dose atropine sulfate aerosol human drugs administered by oral inhalation. FDA is taking this action because alternative products that do not use ODSs are now available and because these products are no longer being marketed in versions that contain ODSs.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2016/10/26/2016-25851/use-of-ozone-depleting-substances)
---
*AI Analytics · CC0 1.0*