myLAB Box COVID-19 At-Home Viral Detection Test

SKU# 29184

myLAB Box COVID-19 At-Home Viral Detection Test

SKU# 29184
3.5 out of 5 Customer Rating
Conveniently test for COVID-19 at home with the myLAB Box P23 COVID-19 At-Home Test. Simply mail in your self-collected saliva sample to a CLIA-certified, high-complexity clinical laboratory for discreet and accurate results.
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Price reduced from $199.99 to $49.99
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myLAB Box COVID-19 At-Home Viral Detection Test
Price reduced from $199.99 to $49.99
  • In Stock
This product is FSA eligible

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Conveniently test for COVID-19 at home with the myLAB Box P23 COVID-19 At-Home Test. The test uses a non-invasive self-collected saliva sample. Self-collection of saliva is painless and helps reduce the risk of spreading COVID-19, compared to collecting deep nasal swabs in a doctor's office or hospital.

Developed by a CLIA-certified high complexity clinical laboratory capable of large volume testing, this test uses polymerase chain reaction (PCR) to detect the COVID-19 virus, if present. The accuracy of this test has been authorized by the FDA under an Emergency Use Authorization (EUA). Take your health to the next level with guaranteed FSA eligible Diagnostic products.

Features:

  • Screen for coronavirus (COVID-19)
  • Mail-in kit for home use
  • Viral detection test using saliva sample
  • Gold standard PCR technology
  • Simple collection in 5 minutes or less
  • Results in as little as 24 hours
  • Free physician consult for positives
  • Free overnight shipping included
  • Included: 1 mail-in saliva specimen collection kit


IMPORTANT NOTICE: If you are experiencing symptoms such as shortness of breath (you are having trouble breathing) or a fever greater than 100.4 you should go to your doctor, nearest urgent care or call 911. Do not order this test.

DISCLAIMER  This test has not been FDA cleared or approved. This test has been authorized by FDA under an EUA for use by authorized laboratories. This test has been authorized only for the detection of nucleic acid from SARSCoV-2, not for any other viruses or pathogens. This test 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 authorization is terminated or revoked sooner. This test uses the P23 Labs TaqPath SARS-CoV-2 Assay.

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