Covid TestingCOVID-19 Pre-registered 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.


Get answers fast and minimize time away from school or work by keeping saliva home collection kits at the ready. Pay for test processing or submit to insurance when you activate the kit to use it.




  • Description
  • Additional information


Keep this easy to use, no swab, saliva collection kit for COVID-19 on hand for travel, concerts, events, family gatherings, when you feel ill, or for after you’ve been around someone who is ill.

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 Saliva Covid-19 Home Collection Kit Direct kit on Friday or Saturday, the kit will only sent on Monday
  • If you purchase this Saliva Covid-19 Home Collection Kit Direct kit after 3.30pm, the kit will only be sent the next day.


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 .2 kg
Dimensions 22.86 × 15.24 × 5.08 cm

Billing details

United States (US)

United States (US)

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