Covid-19 & Flu test collection kit uses a non-invasive self-collected saliva or shallow nasal swab sample. Self-collection of saliva or shallow nasal swab is painless and reduces the risk of spreading COVID-19 and Influenza A and Influenza B (Flu A and B) to the public and to healthcare providers.
At Home COVID-19 Saliva PCR Test EXPRESS OVERNIGHT SHIPPING
COVID & Flu / At-Home Wellness & Nutrition The at home Covid 19 test helps to determine whether or not you may have coronavirus.
The myLAB Box P23 COVID-19 At-Home Test offers a convenient and safe way for people to test for COVID-19 infection. The test uses a non-invasive self-collected saliva sample. Self-collection of saliva is painless and reduces the risk of spreading COVID-19, compared to collecting deep nasal swabs in a doctor’s office or hospital.
Your test kit(s) will be shipped the next day for all orders completed by 11:00 AM CST Monday - Thursday (AK and HI are second-day shipping where Next Day is not available). Orders completed after 11:00 AM CST on Friday or Saturday will deliver on Monday. Orders completed after 11:00 AM CST on Sunday will deliver Tuesday.
The test kit was developed by a CLIA-certified high complexity clinical laboratory capable of large volume testing. The lab uses gold standard PCR to detect the COVID-19 virus if present. The accuracy of this test has been validated and is authorized by the FDA under an Emergency Use Authorization (EUA).
Upon receipt of your kit in the mail, collect your sample following the instructions provided in the kit and send your sample to the lab using the prepaid overnight return envelope provided in the kit.
IMPORTANT NOTICE: If you have any symptoms of a serious COVID-19 infection such as difficulty breathing or shortness of breath, persistent pain or pressure in the chest, new confusion, or inability to arouse or bluish lips or face, please do NOT order a test for COVID-19. Please instead contact your healthcare provider immediately, and failing to reach them, go to the nearest emergency room or dial 911 for medical assistance.
For more details, please refer to the myLAB Box P23 At-Home COVID-19 Test Collection Kit Saliva – Unsupervised - Instructions for Patients
Included: 1 mail-in saliva specimen collection kit
Here’s how it works:
- Order the herpes home testing kit online. They are shipped free and with discreet packaging.
- Secure a sample using the easy-to-follow instructions. We include everything you need to collect your specimen in the testing kit.
- Return your kit for testing using the provided prepaid envelope, which includes free shipping too.
- Receive lab-certified results within 2 to 5 days online.
- Make an appointment for your free phone consultation with a doctor to review your test results if you receive a positive.
Testing for herpes has never been easier. Tests completed from the comfort of your own home! No need to schedule a visit with your physician or visit a lab to test herpes.
At-Home Test Kits powered by MyLabBox only work with the best testing laboratories and health experts. MyLabBox ensures your results meet national standards and are as accurate as tests done in a health clinic or your own doctor’s office.
Labs at the forefront of STD diagnostic testing. MyLabBox partners with certified CAP and CLIA high complexity testing organizations. HIPAA web security protocols protect your data.
IVD -For use by people 18 years of age or older. This test kit requires access to the Internet and email account. Not for resale. Intended for sale and use in the U.S. only. Store kit at room temperature. This home collection kit has been authorized by FDA under a EUA. This home collection kit has been authorized only for the home collection and maintenance of nasal swab specimens as an aid in the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens. This home collection kit in combination with the authorized test 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 authorization is terminated or revoked sooner.
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