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COVID-19 Rapid Antigen Test (3 Pack)

$19.99

Pack of 3 Flowflex COVID-19 Official Emergency Use Authorized 15 minute rapid antigen test kits.

Each order placed includes 3 individually boxed genuine COVID-19 antigen tests.

Ships within 24 hours of order placement.

Guaranteed Genuine

IN STOCK NOW!!

SKU: FLOWFLEX101 Category:

Description

COVID-19 Rapid Antigen Test Kit – FlowFlex – 3 Individually Boxed Tests

Each test is individually packaged in its own box

Find peace of mind with Flowflex!

  • Easy-to-use nasal swab test
  • Requires just 1 test*
  • Can be used to test children as young as 2 years old
  • For use with and without COVID-19 symptoms
  • Accurate results in 15 minutes
  • No need to send off to a lab to obtain results
  • Compact packaging for “On-The-Go” testing

*Other COVID-19 antigen home tests may require a 2nd test 2-3 days after the first.

Get Back to Sharing Special Moments

with Family and Friends

The Flowflex COVID-19 Antigen Home Test is all you need to determine your family’s COVID-19 status.

Critical Information When & Where You Need It

The Flowflex COVID-19 Antigen Home Test is all you need to determine your family’s Covid-19 status, whether symptoms are present or not. Can be used on children as young as 2 years old. Get the convenience of Flowflex!

  • Easy and Affordable
  • Highly Accurate Nasal Swab Test
  • Quick Results in 15 minutes
  • Safe for children as young as 2 years old
  • For use with and without symptoms

 

Test Procedure Overview

 

 

This test procedure overview does not replace the package insert. Before you begin the test, it is important to read and follow the detailed instructions in the package insert.

 

 

This product has been authorized by FDA under an EUA. This product has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens.  The emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of IVDs 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.

 

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