BinaxNOW™ COVID-19 Antigen Self Test

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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.

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The same technology doctors use to test for COVID-19.

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Detects multiple variants.

Learn more about different types of rapid respiratory testing.

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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.

Reliable COVID-19 results in just 15 minutes.

The same technology doctors use to test for COVID-19.

Detects multiple variants.

Learn more about different types of rapid respiratory testing.

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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.

Play video

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 | SPANISH

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

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

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Stick the swab through the
bottom hole into the top hole. Turn the swab to the right clockwise 3x. Fold the card.

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

EXPIRATION DATE EXTENSION

Since the launch of the BinaxNOW™ COVID-19 Antigen Self Test, Abbott has continued testing for product stability to extend the expiration date and have shared these results with the FDA. Testing has been completed to support a shelf-life (expiration date) of up to 22 months. The BinaxNOW™ COVID-19 Antigen Self Test, part number 195-160 or 195- 180, may now have a longer than labeled product expiry date. All BinaxNOW COVID-19 Antigen Self Test kits currently have a twenty-two-month expiry date.

ENTER YOUR LOT NUMBER:

KIT LOT NUMBERORIGINAL PRINTED EXPIRATION DATE ^ EXTENDED EXPIRATION DATE

Disclaimer:

This tool is designed to offer a convenient way for consumers to lookup extended dating by lot number, utilizing information shared by Abbott with the FDA. For official information, please see the FDA letter listing BinaxNOW™ COVID-19 Antigen Self Test kit lot numbers, currently labeled kit expiry and new kit expiry date available on the FDA website at https://www.fda.gov/media/158003/download.

Where to find your lot number on your test kit box:

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Note: do not use LOT number on individual kit components (test cards, nasal swabs, reagent bottles, instructions, or fact sheet)

read more about
rapid testing

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FIND THE BEST TEST FOR YOU

Rapid tests are essential tools to help diagnose what’s behind your symptoms, so you can treat earlier and get well sooner. Understand the differences between rapid molecular tests and at home COVID-19 antigen self tests.

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Sign up for Rapid Insights, our email series on rapid molecular 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.

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ALL ABOUT RESPIRATORY ILLNESSES

Learn about respiratory illnesses and the newer advanced test technology that offers fast and accurate results. Knowing now means you’ll be treated earlier which can help you 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.

*1H 2023 Nielsen Test Sales Market Data on file

**Abbott conducted a computational analysis of the detection of multiple SARS-COV-2 strains, including the OMICRON variant, and predicts no impact in the performance of our BinaxNOW COVID-19 Antigen Self Test.

^Some kits may have an additional label added that states “New expiry date. Disregard dates printed on components.” Original printed expiration date may be covered by this new label.

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