The iHealth COVID-19 & Flu A&B 3-in-1 test redefines at-home diagnostics by combining the ability to detect COVID-19, flu A, and flu B in a single, easy-to-use kit. Designed with precision and reliability, this rapid test delivers peace of mind with accurate results in just 15 minutes, empowering families to make informed health decisions quickly and conveniently.
Product Details:
FDA Authorized 15-Minute Flu A&B, COVID Test Kit:
Over-the-counter flu and COVID test for home use with c
Made for Ages 2 and Above; Parents Can Stop Guessing: Quickly identify whether you or your kids are dealing with coronavirus or influenza A & B. Adult-collection is required for those aged 2-13 years, and self-collection by individuals aged 14 years and older.
Same Ease-of-Use; Get 3 Results in 1 Test: Utilizing the familiar 4 user-friendly steps of at-home COVID tests, you can now get all 3 results for COVID-19 and Flu A & B at once with 5 drops of sample.
Fast and Convenient COVID and Flu Tests for Home: Use this COVID and influenza rapid test kit in the comfort of your home. Bypass the need for a doctor's visit and protect your loved ones from potential exposure to contagious illnesses at school, work, or public gatherings.
Compact Design for On-the-Go Testing: Stay safe wherever you go with our COVID-19, Flu A & B 3-in-1 self-test. Its compact design ensures easy storage and convenient portability for your travel bag.
Suggested Use:
For complete direction, please reference the Instructions Manual. Kit Contents: 5*Nasal Swabs 5*Test Cards 5*Pre-Filled Tubes. Items necessary to use the test but not provided in the test kits: timer or clock. Use immediately after opening the foil pouch. Avoid contact of the extraction solution in the Test Tube with skin and eyes. For more information about current expiration dates for at-home OTC COVID-19/influenza diagnostic tests, please visit: http://www.fda.gov/covid-tests
Patient User instruction:
https://www.fda.gov/media/178554/download?attachment
Ingredients:
Not applicable
Warnings:
In the USA, this product has not been FDA cleared or approved, but has been authorized by FDA under an Emergency Use Authorization (EUA). This product has been authorized only for the detection of proteins from SARS-CoV-2, influenza A, and influenza B, 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 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.§360bblr3(b)(1), unless the declaration is terminated or authorization is revoked sooner. Persons with risk factors for severe disease from respiratory pathogens should consult and follow-up with a healthcare provider. Determining a negative result requires multiple tests. You may need to purchase additional tests to perform serial (repeat) testing. This test is more likely to give you a false negative result when you have COVID-19 than a lab-based molecular test.
