Global Point of Care

BinaxNOW™ COVID-19 Antigen Self Test

Stay ready with the same technology doctors use to test for COVID-19.

Conveniently sold just about everywhere.

Order the #1 COVID-19 self test in the US* by tapping your favorite place to shop below.

The #1 COVID-19 self test in the US.
Made right here in the US.

During the early stages of the pandemic, we helped pioneer the technology used on the frontlines to test for COVID-19.
Now that same technology is available to you in a convenient at-home testing kit.

15 minutes
Reliable COVID-19 results
in just 15 minutes.
same-tech
The same technology doctors use
to test for COVID-19.
fas-hsa
FSA/HSA eligible**

Learn more about different types of rapid respiratory testing.

How it works?
Very well actually.

You don’t need to be a doctor to figure out the same technology doctors use to test for COVID-19.
Watch this video to see how the BinaxNOW COVID-19 Self Test goes down.

Get reliable COVID-19 results in 15 minutes.

Please consult the full illustrated instructions included in your kit when taking the test.

PDF Instructions: English Español

dsfsdf

Open the test card and apply six drops to the top hole only.

dsfsdf

Give both nostrils a shallow swab for about 15 seconds on each side. Big circles – no spinning!

dsfsdf

Stick the swab through the bottom hole into the top hole. Turn the swab to the right clockwise 3x. Fold the card – it should look like a lollipop when you’re done.

dsfsdf

Wait 15 minutes to see your reliable COVID-19 results.

respiratory solution

RAPID RESPIRATORY TESTING INFORMATION FOR CONSUMERS

From corner pharmacies to local urgent care clinics, our rapid respiratory test products are widely available. 

CRM

SIGN UP FOR RAPID INSIGHTS, OUR EMAIL SERIES ON RAPID tESTING.

This program will teach you about rapid tests and how they can quickly identify illnesses like the flu, COVID-19, RSV, and strep throat. Rapid testing can help you get treated earlier and get well sooner.

Only available in the US. Terms of Sale.

The BinaxNOW™ COVID-19 Antigen Self Test has not been FDA cleared or approved. It has been authorized by the FDA under an emergency use authorization. It has been authorized only for the detection of proteins from SARSCoV-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. 

*2022 Nielsen Test Sales Market data on file

**Contact your health insurance provider to determine reimbursement eligibility