Avaliable on the Appstore Avaliable in Android Market / Google Play
Avaliable on the Appstore Avaliable in Android Market / Google Play
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$14.97 2, 4, or 180 Pack: 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 +FS

1Sale offers 2, 4, or 180 Pack: 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 for $14.97 +Free Shipping

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Editor's Note: These are in stock in our Florida Warehouse. While the expiration date on the box shows June 23, 2022, iHealth extended all Covid Rapid Tests an additional 9 months. Therefore, the true expiration date of these tests is March 23, 2023. This extension letter can be found via the following link on the FDA's website: https://www.fda.gov/media/157340/download

ALL SALES ARE FINAL

  •  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.
  • The iHealth COVID-19 Antigen Rapid Test is a lateral flow assay intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2.
  • Easy to Use with Zero Discomfort: 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 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.

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.

Category: Beauty & Personal Care

Posted on 10 May 2022, 03:08 PM
1Sale Deals
posted by 1Sale Deals
10 May 2022, 03:08 PM