iHealth COVID-19 Antigen Rapid Test, 2 Tests per Pack,FDA EUA Authorized OTC At-home Self Test, Results in 15 Minutes with Non-invasive Nasal Swab, Easy to Use & No Discomfort
What are ihealth covid-19 antigen rapid test features?
- Make sure this fits by entering your model number.
- Expiration date extension: on july 8, 2022, 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 12 months. Please refer to the fda website for the detailed list of extended expiration dates by lot numbers: https://www.fda.gov/media/158007/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.
Product guides and documents
iHealth COVID-19 Antigen Rapid Test, 2 Tests per Pack,FDA EUA Authorized OTC At-home Self Test, Results in 15 Minutes with Non-invasive Nasal Swab, Easy to Use & No Discomfort AMAZON
Looking for specific info?
How is it no one has asked the key question: what are verified rates of false-negatives or false-positives?
See less
Is there an expiration date?
See less
Will this test satisfy us governmental requirements for airplane travel?
See less
What is the shelf life of the kits after shipment? (not after manufacture — they don’t do much good if they expire waiting to be shipped.)
Fda extension letter could be found from here:
https://www.fda.gov/media/157340/download
Did anyone use this test kit successfully detected omicron (confirmed that it is omicron by lab test after the home test was positive)?
Does this test require an app or online account to get my results?
See less
Do you have to give a lot of personal information to use the app or just get an impersonal email?
Product specification says # of items is 1. Does each box come with 2 test items for 2 tests within 36 hrs testing process for this product?
Will this be able to detect if i’ve had covid at any point, or only if i’m currently infected?
Are the swabs processed with ethel oxide?
My nasal passages are really dry. Will i be able to get a sample sufficient for this test? Any tips?
If i’m sick now and it won’t arrive for 15 days, is it worth it?
Does this detect omicron?
What is the national drug code number? This number is needed for reimbursement for the tests through health insurance in the united state.
2. Ndc code: 56362-0005-89
hope these information is good for you.
See less
Could you use your own q-tip to collect the sample?
Does the sterile swab have eo on the packet?
How much solution should be in the vials? I have about 3/8 inch.
Anyone get a refund or replacement for missing solution?
What is the tax code number to file for reimbursement?
See less
What is the rx and prescription number for the ihealth covid 19 antigen rapid test? Need to submit for reimbursement.
See less
iHealth COVID-19 Antigen Rapid Test, 2 Tests per Pack,FDA EUA Authorized OTC At-home Self Test, Results in 15 Minutes with Non-invasive Nasal Swab, Easy to Use & No Discomfort AMAZON
What are our customers saying?
Important informationLegal Disclaimer
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.