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BinaxNOW COVID-19 Antigen Self Test, COVID Test With 15-Minute Results Without Sending to a Lab, Easy to Use at Home, FDA Emergency Use Authorization

4.4 out of 5 stars 590 ratings

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  • SIMPLE AND EASY TO USE: The BinaxNOW Self Test from Abbott requires just a shallow nasal swab that you can do yourself; includes easy-to-follow instructions
  • SEE RESULTS IN 15 MINUTES: Convenient, fast results anytime, anywhere; no need for a prescription or sending to a lab
  • FOR AGES 2 TO ADULT: The self-test is indicated for children as young as 2 years old when administered by an adult, and for all people 15 and older to self-administer
  • DESIGNED TO DETECT ACTIVE COVID-19 INFECTION: Includes 2 tests that are indicated for serial testing—simply test yourself twice within 3 days, at least 36 hours apart; designed to detect active infection with or without symptoms
  • FOR PERSONAL USE: Does not include a virtual visit for certified digital test results. For proof of negative COVID-19 test, the BinaxNOW COVID-19 Ag Card Home Test may be a better choice.
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From the manufacturer

Product description

BinaxNOW COVID-19 Antigen Self Test from Abbott can be used to detect active infection, with or without symptoms. This rapid-result test is for personal use. See results in just 15 minutes. The box includes 2 tests that are indicated for serial testing—test yourself twice within 3 days, at least 36 hours apart.

Product details

  • Product Dimensions ‏ : ‎ 1.15 x 9.13 x 5.08 inches; 3.17 Ounces
  • Item model number ‏ : ‎ 195-260
  • Date First Available ‏ : ‎ May 18, 2021
  • Manufacturer ‏ : ‎ Abbott Rapid Diagnostics
  • ASIN ‏ : ‎ B094LVQZJL
  • Customer Reviews:
    4.4 out of 5 stars 590 ratings

Important information

Legal Disclaimer

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 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.


Customer Questions & Answers

Customer reviews

4.4 out of 5 stars
4.4 out of 5
590 global ratings
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Top reviews from the United States

Reviewed in the United States on July 4, 2021
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288 people found this helpful
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Reviewed in the United States on July 21, 2021
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5.0 out of 5 stars If you follow the directions, this test will tell you what you need to know.
By Lindsey on July 21, 2021
The first time I took this test, I was in my car, sick, and desperate for an answer. I used too many drop and it tainted my results. I couldn’t see what I was doing since I was in my car trying to use the console as a table. I had a gray line.

The next time I took the test, as pictured, I used the 6 drops as it says and my positive popped up really quick. I wasn’t really having a ton of symptoms, so I feel it detected it early for me.
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220 people found this helpful
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Reviewed in the United States on June 29, 2021
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186 people found this helpful
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Reviewed in the United States on July 3, 2021
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167 people found this helpful
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Reviewed in the United States on July 5, 2021
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1.0 out of 5 stars Bad
By T on July 5, 2021
Box was unsealed. Disgusting.
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138 people found this helpful
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Reviewed in the United States on July 20, 2021
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139 people found this helpful
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Reviewed in the United States on July 19, 2021
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127 people found this helpful
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Reviewed in the United States on July 1, 2021
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113 people found this helpful
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