Covid TestingCOVID-19 PCR Test


No swab, saliva, home collection kit for PCR COVID-19 test offers convenient and easy identification of SARS-CoV-2 infection in both symptomatic and asymptomatic individuals.


This option is billed to commercial or federal insurance programs for eligible individuals who are sick, have potential exposure to COVID-19, live/work in a congregate setting, or have a doctor’s order.








  • Description
  • Additional information


This $0 down option is meant for individuals who are experiencing COVID-related symptoms, have possible exposure to COVID, live/work in a congregate setting, or have a doctor’s order. If you do not have insurance, the test will be submitted for federal insurance.

Simply activate the kit online using with the enclosed activation card before sending it to the lab using the pre-paid, overnight return shipping packaging. You will receive your results through our HIPAA- compliant online portal within 24 hours of when the lab receives the kit.


  • No swab, saliva collection
  • FDA authorized
  • Meets strict travel requirements
  • Reimbursable by insurance
  • Pre-paid overnight shipping and packaging
  • Results in 24 hours or less
  • HIPAA-compliant, online portal access to results

Kit Contents

  • 1- Collection instruction
  • 1- Kit activation card
  • 1- Labeled screw-cap tube with funnel
  • 1- Patient identifier sticker
  • 1- Alcohol pad
  • 1- Biohazard bag with absorbent pad
  • 1- SalivaDirect box for return shipment
  • 1- FedEx pak with pre-applied, pre-paid shipping label

Important Note:

  • If you purchase this kit after 3:00 pm ET, Monday-Friday, the kit will be sent the next business day.
  • If you purchase this kit on Friday after 3:30 ET or on Saturday, the kit will be sent on Monday.


This test has not been FDA cleared or approved; This test has been authorized by FDA under an Emergency Use Authorization (EUA) for use by authorized laboratories. This test has been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens.

This test 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 authorization is terminated or revoked sooner.








Additional information

Weight .8 kg
Dimensions 22.86 × 15.24 × 5.08 cm

Billing details

United States (US)

United States (US)

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