“Delta is the most infectious virus ever seen” - CDC
"Delta Strain as Contagious as Chickenpox"
“Fully vaccinated people becoming symptom free Super Spreaders”
“Vaccinated people infected and getting sick”
You Would be a Fool Not to be Worried
The above headlines sent chills up and down my spine. I always knew the Delta strain is a highly contagious killer... but to see it confirmed in black and white is my worst nightmare
The Abbott BinaxNOW COVID-19 Antigen OTC Home Test lets you get rapid results, in the privacy of your own home. Available direct from us at Salvavida, everything you need is in the package and taking the test is simple.
The Abbott BinaxNOW COVID-19 Antigen OTC Home Test utilizes trusted technology used for decades by healthcare professionals and makes simple, easy-to-use COVID-19 tests easily accessible. This has been a game changer for us. Life around here is now near normal. The best it's been in two years... Since this horror show started.
Features/Benefits: When it comes to COVID-19, knowledge is power. People want to know if they are infectious or not and they want their results now.
Rapid tests are best at detecting higher amounts of viral load when people are most likely to be infectious. And they deliver results quickly enough to help sick individuals from potentially spreading the virus to others. With multiple rapid tests available, what should you look for when selecting a rapid test?
Speed: Look for tests that offer results in minutes, not hours or days. Tests claiming to be "rapid" but still require mail-in samples or lab processing times have delays built in. Our BinaxNOW COVID-19 tests deliver results in 15 minutes or less.
Convenience: Testing that's convenient and accessible is likely closer to you. Tests that don't require instrumentation can be performed at home (with a virtually guided service) or outside of traditional healthcare settings, in drive-thru clinics, schools, workplaces and stand-up community testing sites. Look for tests offered in myriad locations.
Comfort: Nasal swabs that don't require a deep swab are the most comfortable. They're preferable to nasopharyngeal swabs, which can be uncomfortable and require that healthcare workers take additional precautions.
Reliability: Our BinaxNOW test is among the most studied rapid antigen test in the country and demonstrates performance of 95.6% positive agreement (sensitivity) in people seven days or less post-symptom onset with Ct counts of 33 or below. These are people who are most likely to be infectious and spread the virus to others.
Track Record: All COVID-19 tests in the U.S. have been authorized under FDA Emergency Use Authorization. Abbott's rapid tests are among the most widely-used in the U.S., with more than 200 million of our BinaxNOW rapid tests used in urgent care clinics, doctor's offices, pharmacies, nursing homes, and schools since April 2020.
Our Rapid COVID-19 Tests
Our BinaxNOW test is the size of a credit card and requires no specialized instrumentation. This sleek form factor is what allows us to make it at scale and sell it at an affordable price. The test can be used at home without a prescription and through a virtually guided online video. This test kit is extremely easy to use.
Even as promising vaccines become more widely available, reliable, quick and convenient rapid testing will play an important role in containing pockets of infectious mutations that are in some cases defeating vaccinations.
Home testing is helping people get back to business, travel, school and visiting loved ones.
Because the sooner your COVID results are known, the sooner you can get back to the things you want to do. And now, you're ready.
If you’d like to see an instructional video, scan the QR code below
*Prices subject to change. Better hurry supplies are limited and flying out the door!
The Abbott BinaxNOW COVID-19 Antigen OTC Home 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.