FDA allows pharmacies to produce alcohol-based hand sanitizers amid shortage

Aileen Cerrudo

The Food and Drug Administration (FDA) has allowed pharmacies to produce their own alcohol-based hand sanitizers to cope with the supply shortage.

According to the FDA, there has been an increase in the demand for alcohol-based products amid the increasing threat of the coronavirus disease (COVID-19) in the country.

Based on FDA Circular No. 2020-11, licensed drug stores, hospital pharmacies, institutional pharmacies, and other stakeholders will be allowed to produce their own alcohol-based hand sanitizers for consumer and health care personnel use.

The FDA also provided several guidelines to ensure pharmacies will produce safe, effective, and acceptable quality alcohol-based products for public use.

Several of the guidelines include: the compounding should be done by a duly registered and licensed pharmacist. They would also have to follow strict hygiene and personal protective equipment requirements.

The location for the compounding, including all the equipment should also be properly sanitized and maintained.

“This Circular is hereby issued as an interim guideline for the pharmacy compounding of alcohol-based hand sanitizers in response to the need for increased production of these products in the Philippines,” the circular reads. AAC

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