BinaxNOW COVID‐19 Antigen Self Test
From: $200.00
BinaxNOW COVID‐19 Antigen Self Test
Product Type: | Rapid COVID Tests |
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Product Name: | COVID-19 Antigen Self Test |
Brand: | BinaxNOW |
FSA Eligible: | Yes |
Size/Count: | 2.0ea |
Item Code: | 917187 |
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Description
BinaxNOW COVID‐19 Antigen Self Test
- BinaxNOW 2-Test Pack: This double-pack includes 2 at-home tests designed to detect active infection.
- BinaxNOW™ Self Test uses THE SAME TECHNOLOGY USED BY DOCTORS to test for COVID-19.
- Detects multiple COVID-19 variants, including Delta and Omicron*
- FDA Authorized 15-Minute Self Test: Convenient COVID-19 at-home test provides fast, reliable results in 15 minutes, results anytime, anywhere; no need for a prescription or to send to a lab.
- Reliable and Easy-to-Use: Requires just a shallow nasal swab that you can do yourself; includes easy-to-follow instructions.
- For Ages 2 and Above: COVID test suitable for kids, when administered by an adult, and for all people 15 and older to self-administer.
- So precaution should be highly considered when taking this drugs and to patient when administered
- Revert to our safety precaution measures and contact us for your daily guidance when taking BinaxNOW COVID‐19 Antigen Self Test drugs.
The FDA has not cleared or approved the BinaxNOW™ COVID-19 Antigen Self Test. The FDA has authorized it under an emergency use authorization.
It has been authorized only for the detection of proteins from SARSCoV-2, not for any other viruses or pathogens, and 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, 21U.S.C. § 360bbb-3(b)(1), unless the declaration is terminated or authorization is revoked sooner.
Warnings
The test has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens, and is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostic tests 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.
Additional information
Quantity | 8 COVID 19 Test, 13 COVID 19 Test, 16 COVID 19 Test, 24 COVID 19 Test, 28 COVID 19 Test, 34 COVID 19 Test, 40 COVID 19 Test |
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