Hand Sanitizer Guidance
If your company is new to making hand sanitizer, our experts can help you understand the U.S. regulatory requirements and get your product on the market.
We guide you through the U.S. FDA’s temporary guidance documents for manufacturing alcohol-based hand sanitizers during the COVID-19 public health emergency. We will assist you with the FDA establishment registration and product listing. If your company is based outside the U.S., we can also act as your U.S. agent.
Our experts provide guidance and help you get your hand sanitizer product to the market. Our experts:
- Help you navigate through the U.S. FDA’s temporary guidance for manufacturing alcohol-based hand sanitizers during the COVID-19 public health emergency
- Register your establishment and list your product
- Act as your U.S. agent if applicable
COVID-19 Hand Sanitizer: Temporary FDA Registration & Listing (511)
U.S.-based companies can purchase this package for FDA establishment registration and product listing.
Learn more or purchase
COVID-19 Hand Sanitizer: Temporary FDA Registration & Listing – Includes U.S. Agent Service (511-A)
If outside the U.S. or needing a U.S. agent, purchase this package for FDA establishment registration/product listing.
Learn more or purchase