iHealth COVID Antigen Test At-Home. EXP 2025

iHealth COVID-19 Test Kit

IHealth Covid 19 Antigen Test Accuracy

• Nasal Swab: 98.8% (95% CI: 97.6%-99.5%) 95% Confidence Intervals
• Saliva: 97.1% (95% CI: 94.6%-98.5%) 95% Confidence Intervals

What Is In The iHealth Covid Test Antigen Home Test Box?

• 2 Test devices: Foil pouched test device containing one test strip which is encased in plastic device cassette with a desiccant
• 2 Extraction vials and caps
• 2 Nasal swabs: swab for anterior nasal specimen collection

How to Use the iHealth Covid 19 Antigen Rapid Test

• Open the kit and remove all items from the test kit.
• Remove the swab from its package and place the entire tip of the swab, up to ¾ of an inch, into one nostril.
• Carefully move the swab in circles at least five times, brushing the insides of the nostril.
• Repeat with the other nostril using the same swab.
• Take the tube, tap it on a table and open the orange cap.
• Place the swab fully into the tube until it touches the bottom, and swirl it in the tube at least 15 times.
• Squeeze the sides of the tube to squeeze out more of the sample from the swab and then throw away the swab.
• Put the cap back on the tube and open the small white cap.
• Squeeze three drops from the tube into the sample well of the test card.
• Wait fifteen minutes to read the results.

EASY TO USE ZERO DISCOMFORT

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Important Documents

• iHealth covid test expiration date extension
• IHealth Fact Sheet
• IHealth Laboratories FDA Emergency Use Authorization
• At-Home Test Instructions For Use
• FDA Extension Letter

• The iHealth™ COVID-19 Antigen Home Test is authorized for non-prescription home use with self-collected direct anterior nasal (nares) swab samples from individuals aged 14 years or older or adult collected direct anterior nasal swab samples from individuals aged two years or older.
• For use under an Emergency Use Authorization (EUA) only for the duration of the COVID-19 declaration justifying the emergency use of in vitro diagnostics (IVD), unless it is terminated or revoked by the FDA (after which the test may no longer be used).

Shipping and Returns Terms and Conditions

How Long Does It Take For My Item(s) To Ship?

Items are shipped Monday – Friday from our warehouse. 1-2 Day Processing Time.

Delivery times vary according to your selected delivery address, the availability of your items, and the time of day you place your order.

Orders placed by 1:00 PM Eastern Time will be shipped the same day from our warehouse. Orders placed after this time will be shipped the next business day.

For B2B accounts, please get in touch with us at [email protected] for urgent order requests.
Please feel free to visit our Support Page for FDA Extension Letters, Submit a Ticket, and more.

What Shipping Methods Do You Offer?

At Peach Medical Corp we use UPS (most orders ship via UPS but some may ship via USPS) as our logistic and Shipping partners. Currently, our shipping methods are as follows:

• UPS Next Day Air (please note UPS Next Day Air delivers your order the next business day. If you order on Friday before 1:00pm EST, the package will be received on Monday)
• UPS 2nd Day Air
• UPS Ground (3-5 Day Delivery)

When Will I Receive My Tracking Number?

Our system updates clients every evening with tracking numbers for their orders. This will be sent via e-mail with an additional copy of your receipt.

Incorrect Address

Please verify your address when ordering, we are unable to fix an incorrect shipping address on an order once it is in transit. If your order is in transit with an incorrect address, please reach out to your carrier to reroute the package. Peach Medical Corp. is not able to have packages rerouted or contact the carrier for you.
No refunds for packages sent to wrong address. Replacement package may be sent if eligible. Contact customer service for more information.

Return Policy and Cancellation Policy

The Peach Medical COVID-19 Antigen Rapid Test and face masks are personal items. Therefore, they cannot be returned or refunded. Replacement may be shipped if the item is defective. Proof of purchase, photos of defects, lot numbers, and other information are required to authorize a replacement. Please reach out to customer service for detailed requirements before disposing of the defective units. We will not replace your COVID-19 Antigen Rapid Test kits that are expiring soon based on the printed label. Our expiration dates have been shown on each product page. More information can be found at support.peachmedical.com/portal/en/kb/peachmedicalsourcing.

We will continue to update the FDA documents for shelf-life extensions for our tests.
If a customer chooses a 3rd party receiver who is not the purchaser, Peach Medical is not responsible for any goods once they leave our warehouse and when tracking is provided. I.e Gifts, International Shipping Services. All Products must be packed in the original, unopened, and unmarked packaging including any accessories, manuals, documentation, and registration that shipped with the Product.
Note: If Peach Medical has not shipped your item within 7 business days, cancellations will be honored. Please email us at [email protected] for return authorization and the shipping address.</P

IHealth COVID-19 Rapid Test Frequently Asked Questions

How does the IHealth COVID-19 Antigen Rapid Test work?

The iHealth® COVID-19 Antigen Rapid Test is an antigen test. When COVID-19 is present in the body, your nasal secretions can also contain the SARS-CoV-2 virus (the virus that causes COVID-19). The iHealth® COVID-19 Antigen Rapid Test can detect small parts of the SARS-CoV-2 virus, known as N protein or antigens, in your nasal secretions.

Will this test detect COVID-19 variants?

The iHealth COVID test has completed testing on several heat-inactivated variant strains and the iHealth® COVID-19 Antigen Rapid Test was able to detect the mutations. The clinical performance has not been established in all circulating variants but is anticipated to be reflective of the prevalent variants in circulation at the time and location of the clinical evaluation. Performance at the time of testing may vary depending on the variants circulating, including newly emerging strains of SARS-CoV-2 and their prevalence, which change over time.

Is this iHealth COVID-19 Antigen Rapid Test Kit FDA approved or cleared?

No. This test is not yet approved or cleared by the United States FDA. FDA can issue an Emergency Use Authorization (EUA) when certain criteria are met, which includes that there are no adequate, approved, available alternatives. The EUA for this test is supported by the Secretary of Health and Human Services’ (HHS’s) declaration that circumstances exist to justify emergency use of in vitro diagnostics for the detection and/or diagnosis of the virus that causes COVID-19. This EUA will remain in effect (meaning this test can be used) for the duration of the COVID-19 declaration justifying emergency of IVDs, unless it is terminated or authorization is revoked by FDA (after which the test may no longer be used).

What is the age range for the test?

This test is authorized for nonprescription home use with self-collected (unobserved) anterior nasal swab specimens from individuals aged 15 years and older or with adult-collected anterior nasal swab samples from individuals aged 2 years or older.

What is serial testing?

Serial testing is when a single person is tested for COVID-19 more than once. Because antigen tests are less sensitive than other COVID-19 tests and false results may occur, repeated testing may identify individuals with COVID-19 more reliably than a single test. By repeating testing, it may be possible to more quickly identify cases of COVID-19 and reduce spread of infection. Additional testing with molecular COVID-19 tests may be necessary, depending on your individual risk factors and test results. It is important that you work with your healthcare provider to help you understand the next steps you should take. Serial testing (i.e., testing every day or every other day) is more likely to detect COVID-19, especially when you do not have any symptoms. Testing for asymptomatic individuals should be performed at least twice over three days, with at least twenty-four hours and no more than 48 hours between tests. You may need to purchase additional tests to perform this serial (repeat) testing.

Do I always need to perform two tests?

If you have COVID-19 symptoms and are within the first 7 days of symptom onset, you can use one single test of the iHealth® COVID-19 Antigen Rapid Test. You may also choose to perform two tests if you wish. By testing more frequently, you may detect COVID-19 more quickly and reduce spread of infection. If you do not have COVID-19 symptoms or have been having symptoms for more than 7 days, you will need to perform two tests over two or three days with at least 24 hours and no more than 48 hours between tests.

How accurate is the iHealth COVID-19 Antigen Rapid Test?

Based on the results of a clinical study where the iHealth® COVID-19 Antigen Rapid Test was compared to an FDA authorized molecular SARS-CoV-2 test, the iHealth® COVID-19 Antigen Rapid Test correctly identified 94.3% of positive specimens and 98.1% of negative specimens. Additional asymptomatic individuals and individuals beyond the seven days of symptom onset were tested, but excluded from the primary performance calculations because they were not included in the intended use. A higher proportion of low positive specimens were observed in these populations, resulting in PPAs between 85-88% in these individuals.