New variants have shown that anyone can be vulnerable to COVID-19 even if they are vaccinated or young. With iHealth COVID-19 Antigen Rapid Test, you can test yourself after being out in public. Early and regular testing helps you better care for yourself and protects your friends, family, and community members from potential exposure.
4 Steps. 15 Minutes. Zero Discomfort.
iHealth COVID-19 Antigen Rapid Test is the simplest way to detect SARS-CoV-2 nucleocapsid protein antigen. It only takes 4 steps and 15 minutes to complete the test. The test is also non-invasive. You won't need to collect a sample from deep in your nasal cavity to get accurate results.
Flu or COVID, 15 mins to get peace of mind.
In case of physical discomfort such as fever, sneezing, cough or fatigue, you can quickly detect SARS-CoV-2 nucleocapsid protein antigen by using iHealth COVID-19 Antigen Rapid Test.
Quick in-home testing takes away the worry of developing symptoms.
Back to school, back to the office, or just back from travel or public gatherings, a rapid,15-minute, self-test is waiting at home for when you get back.
An in-home test designed to get results in 15 mins.
Not only is the iHealth COVID-19 Antigen Rapid Test easy and non-invasive, it’s a small engineering beauty. The test has a highly-absorbent swab that is individually sealed to help prevent contamination so you can view the results of your in-home test with confidence.
Highly-Absorbent swab
Made of PU foam, the absorbent tip of the swab makes sample collection more efficient than a regular swab.
Double-Cap Security Design
The double-cap design allows you to safely store the liquid and then precisely drip the mixed sample onto the test card.
Easy-to-Understand Results
The unique test card shortens the time to get your results and makes them easy to read. If only the C line shows up, the test is negative. If both C and T lines show up, the test is positive.
Product Benefits
Expiration Date Extension: On Jan 11, 2023, the FDA granted another three-month shelf-life extension for the iHealth COVID-19 Antigen Rapid Test, which extended the shelf-life of all iHealth tests from 6 months to 15 months. Please refer to the FDA website for the detailed list of extended expiration dates by lot numbers: https://www.fda.gov/media/164551/download
FDA Authorized 15-Minute Self-Test: The test is a 15-minute self-test to detect whether or not an individual has COVID-19. The test can be completed in the comfort of your own home without the need to ship your sample to a lab.
Easy to Use with Zero Discomfort: The test can be done by inserting 1/2 to 3/4 inch of a simple non-invasive nasal swab. Step-by-step instructional videos are available in our app (Installation of the app is optional).
For Ages 2 and Above: The self-administered test is recommended for individuals aged 15 years and older. Adult-collection is required for testing children 2-14 years old.
Manage Group Testing Via Mobile App: The iHealth Test app allows the administrator of a small group to monitor and track the group members’ test results as needed at school, work, or an event.
Result Time: 15 min
Features: Disposable, Fast Results
Instructions for Use
1. Swab
Brush against the inner wall of both nostrils 5 times each in a circular motion with a non-invasive nasal swab. Our nasal swab is soft, highly absorbent, and only needs to be inserted ½ - ¾ inches so you can test yourself comfortably.
2. Dip
Insert the swab with the sample into the bottom of the tube and stir it in the fluid 15 times. Squeeze the sides of the tube around the swab as you pull it out.
3. Drip
Put 3 drops of the mixed solution onto the sample port of the COVID-19 test card.
4. Wait 15 minutes
Start the timer. Your results will be ready in 15 minutes.
Instructions
Store iHealth COVID-19 Antigen Rapid Test in a dry place between 36-86 F (2-30 C). Ensure all test components are at room temperature 65-86 F (18-30 C) before use.
Legal Disclaimer
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. § 360bbb-3(b)(1), unless the declaration is terminated or authorization is revoked sooner.
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