COVID-19 Home Test
iHealth COVID-19 Antigen Rapid Test
$18.99
- 2-3 Day Delivery
- 2 Per Box
About iHealth Home Test
IHealth COVID-19 home test is an effective test kit, proudly offered by CoviLab for the detection of SARS-CoV-2. It is a lateral flow immunoassay designed to qualitatively detect nucleocapsid protein antigens (SAR-CoV-2) from respiratory samples like nasal swabs or saliva. It’s effective for self-testing within 7 days of COVID-19 symptoms manifestation. With this test kit, serial testing can be performed over 3 days while ensuring gaps of 24 to 48-hours in-between tests.
IHealth home test kit is completely safe. It is authorized as non-prescription use under the FDA’s Emergency Use Authorization (EUA). This is the perfect solution if you ever suspect COVID-19 infection. With IHealth, complete your 15-minutes self-test and determine your COVID-19 status within minutes.
Monitor Your Health Regularly
Features:
- Easy-to-use COVID-19 antigen test kit
- Less than 15-minutes instant detection
- Integrated with mobile applications for easy result interpretation.
- More comfortable nasal swab sample collection
- Instant identification of current COVID-19 status
- FDA’s EUA authorized.
- For use under Emergency Use Authorization Only
- For In Vitro Diagnostic Use Only
Compatible OS System
- iOS13 or newer for Apple iPhone
- Android10 or newer for Android Phone
IHealth Rapid Test OTC (PDF Info)
Disclaimer:
As of November 22, 2021, iHealth COVID-19 Antigen Home Test is authorized to use with individual anterior nasal swab specimens from individuals age 14 years and older (self-collected), or 2 years and older (collected with adult assistance) for non-prescription home use by FDA under the EUA (EUA210314/S002). The authorized labeling has been changed with the new indication (Quick Reference Instructions (QRI) and Fact Sheet for Individuals, Instructions for Use (IFU) for Healthcare Providers (HCP), Fact Sheet for HCP, and kit package); however, iHealth COVID-19 Antigen Home Test will continue to be distributed with the labeling previously authorized per EUA210314/S001 on the FDA’s enforcement discretion in efforts to increase the testing accessibility for COVID-19. Since the differences between the iHealth COVID-19 Antigen Home Test kit previously authorized (EUA210314/S001) and currently authorized (EUA210314/S002) are limited to the authorized labeling, you may use the iHealth COVID-19 Antigen Home Test kit with the new indication for use (described above).
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Results You Can Trust
CLIA Certified
Non-Invasive Testing
Results In Minutes
Compliant with all Regulatory Standards
Our laboratoy is a proud member of the CLIA program.
Our CLIA-Approved facility is designed specifically to focus on analytes that cause SARS-COV-2 in our local community.
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