NEW

Flowflex® COVID-19
Antigen Home Test

A Simple Way to Test for COVID-19

ACON Laboratories, Inc. is the only legal manufacturer of the FDA EUA Flowflex COVID-19 Antigen Home Test.

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with Family and Friends

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

Find peace of mind with Flowflex!

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

Expiration Date Extension

As of November 18, 2022, the expiration date of the Flowflex COVID-19 Antigen Home Test has been extended by 9 months. Please click here to check the new expiration date using the lot number printed on the test kit box.

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.

Videos

Adult Testing

Adult Testing

Child Testing

Adult Testing

Resources

Consumer Package Insert (English)

Consumer Package Insert (Spanish)

Fact Sheet for Healthcare Professionals

Healthcare Provider Package Insert

Quick Reference Instructions (English)

Quick Reference Instructions (Spanish)

Frequently Asked Questions

Where Can I Buy It?

The Flowflex® COVID-19 Antigen Home Test may be purchased at the following retail drug stores and online:
Costco_Logo

For employee testing solutions, click here.

Looking for a Distributor?

To locate an authorized US distributor, please click the button.

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News

STATEMENT ON THE OMICRON BA.2 VARIANT

We at ACON Laboratories, Inc. have been continuously monitoring the emergence of COVID-19 variants. The Omicron variant (B.1.1.529) is currently the dominant variant circulating globally, accounting fornearly all sequences reported to GISAID. Omicron is made up of...

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UPDATED STATEMENT ON THE OMICRON VARIANT

ACON Laboratories, Inc. has been continuously monitoring the emergence of SARS-CoV-2 variants, including the Omicron variant. We are pleased to report that an independent evaluation conducted by the National Institutes of Health’s (NIH) RADx program has indicated that...

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Headquartered in San Diego, California, ACON Laboratories makes point-of-care medical diagnostics accessible to people around the world. ACON provides rapid diagnostics and healthcare products based on a philosophy of high quality at affordable prices.
  • In the USA, this product has not been FDA cleared or approved; but 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; and,
  • 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 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. § 360bbb3(b)(1), unless the declaration is terminated or authorization is revoked sooner.

For more information on EUAs please visit: https://www.fda.gov/emergency-preparedness-and-response/mcm-legal-regulatory-and-policy-framework/emergency-use-authorization

For the most up to date information on COVID-19, please visit: www.cdc.gov/COVID19