Abbott BinaxNOW™ COVID-19 Ag Card Home Test, Enabled by

Order as few as 1,224 tests (minimum 1 pallet) | $25/test

Get back to life and meet your organization's COVID-19 compliance requirements with the Abbott BinaxNow™ COVID-19 Home Tests. It’s the first FDA-authorized, virtually guided, at-home COVID-19 rapid test with automated results reporting. Live testing support from eMed Certified Guides ensures better sample collection and improved confidence in results.

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Abbott BinaxNow Covid-19 Ag Home Test
Abbott BinaxNow Covid-19 Ag Home Test in Bulk
BinaxNow Covid-19 Ag Home Test
Covid-19 Ag Home Test in Bulk

About BinaxNOW™

Developed by Abbott, the BinaxNOW test is an at-home solution that utilizes a digital point-of-care platform from eMed to virtually guide the user through the test process from beginning to end. The test delivers results in just 15 minutes with no instrumentation, using proven lateral flow technology.

NAVICA, Abbott’s complementary smartphone app, allows users to display their BinaxNOW test results when asked by organizations where people gather, such as workplaces, schools, events, and when traveling.

Why Abbott BinaxNOW™ for your team?

  • Most widely-used end-to-end Covid-19 testing solution developed by Abbott Laboratories and enabled by eMed
  • FDA Emergency Use Authorization (EUA) received
  • Results reporting in 15 minutes
  • Test sensitivity of 97.1% and specificity of 98.5%
  • Third-party verification ensures authentication
  • Digital Health Results sent to mobile app with Digital Health Pass or Guide To Care Instructions
  • 24/7 Live Support – eMed certified guides & customer support agents

How It Works

Virtual Test Guidance through eMed Certified Guides

Place your order with an iPromo representative, then an eMed Healthcare Partner will grant a prescription if qualified and your order will be shipped. A live, virtual eMed Certified Guide instructs users to scan the test’s QR code, leads them through the testing process, and reads the test result. This certified authentication and guided administration helps optimize testing success and reporting integrity.

Abbott also offers NAVICA, a complementary smartphone app, which allows you to display Abbott's BinaxNOW test results when asked by organizations where people gather, such as workplaces and schools, and for travel.

Frequently Asked Questions

How do you take a sample?

Self-collect your sample from home following the instructions provided during the video visit with an eMed Certified Guide. Collecting a sample is an easy to follow and gentle process, no different to using a cotton swab to clean the inside of your nose.

What happens if I receive a positive result?

If you receive a positive result you should remain in self-isolation, and inform your healthcare provider of your result. You should follow the guidance provided by the Centers for Disease Control and Prevention (CDC).

If you develop emergency warning signs for COVID-19, get medical attention immediately. Emergency warning signs include*:

  • Difficulty breathing or shortness of breath
  • Persistent pain or pressure in the chest
  • New confusion or inability to arouse
  • Bluish lips or face

*This list is not all inclusive. Please consult your medical provider for any other symptoms that are severe or concerning.

What does FDA authorized mean?

Abbott's BinaxNOW COVID-19 Ag Card Test has been issued an Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA) for prescription home use, which provides consumers with the ability to test themselves from the comfort and safety of their homes.

When there is a critical situation impacting health and safety and there are no FDA-approved or cleared tests available, and other criteria are met, the FDA can make tests available under an emergency access mechanism called an Emergency Use Authorization (EUA). The EUA for this test is supported by the Secretary of Health and Human Service’s (HHS’s) declaration that circumstances exist to justify the emergency use of in vitro diagnostics for the detection and / or diagnosis of the virus that causes COVID-19.

What does Sensitivity 91.7% and Specificity 98.5% mean?

In a diagnostic test, Sensitivity is a measure of how well a test can identify true positives. In a diagnostic test, Specificity is a measure of how well a test can identify true negatives.

How do I place a bulk order for my organization or institution?

For bulk order inquiries, please fill out the quote form at the top of this page with as much detail as possible pertaining to your request.


  • Test authorized for use by persons age 4+.
  • Test takers 14 or younger must be accompanied by an adult during specimen collection.

Enter your contact info and how many tests you need: