Confidence is Minutes Away

During the COVID-19 pandemic, we all learned that keeping ourselves and our families healthy is our highest priority. On/Go™ is here to help. Whether you or someone in your family is feeling ill, has potentially been exposed or needs to demonstrate a negative test result, On/Go is the anytime, anywhere rapid antigen test to have on hand.

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is a solution like no other

By connecting testing with real-time data to keep track of your family and their current status, you'll know you are ready to embark together on the next family vacation, take your child to their sporting events or just be confident when you are visiting your loved ones.

Testing for COVID-19 is important.

Even for those who are fully vaccinated, continued diligence is critical, including the use of rapid antigen testing. As variant strains emerge, the On/Go COVID-19 Self-Test is a great way to remain confident in your health status when:

  • Experiencing respiratory symptoms
  • Traveling abroad
  • Responsible for the health of dependents like elderly parents or unvaccinated children
  • Visiting loved ones in high-risk groups
  • Attending events like concerts or conventions
  • Returning to the office
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The On/Go App

Before You Test, Install the On/Go App

Our easy to use iOS and Android mobile app delivers an intuitive testing experience. The On/Go app provides rapid test results, tracks your testing history and lets you easily share results with those who need to know.

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The On/Go for My Business

Get back to the business of people.

At On/Go we want to empower you to keep your employees safe, show them care and stay open for business. We believe that targeted timely communication, adherence to valid, repeated testing and real-time data provide the best holistic solution for employers and those in their care.

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Disclaimer

This product has not been FDA cleared or approved but has been authorized by FDA under an Emergency Use Authorization (EUA). This product has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens, and is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(1), unless the declaration is terminated or authorization is revoked sooner.