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At-Home Saliva Test for COVID
Results in 72 Hours

For consumers only: Get the answer you need in a few short days—safely from the comfort of home.

Can I Test for COVID-19 at Home?

Yes, you can definitely test for COVID-19 at home. Many people are worried about whether or not they have COVID-19, but don’t feel comfortable risking possible exposure by going to a public place to test. For your peace of mind, DDC is pleased to offer Zero Contact™, a fast, accurate, and convenient COVID-19 test. Just spit into a tube and send it to the lab.
Your results are delivered within 72 hours after sample is received for analysis.

Quick Overview

  • Lab analysis required
  • Accurate results just 72 hours after testing begins
  • For consumers in the U.S.A
Buy Now: $115

About the Product

  • Lab analysis determines if test participant is currently infected with COVID-19
  • FDA-authorized saliva test
  • Customer-friendly process
  • Complete instructions and sample-collection materials included
Buy Now: $115

Quick Overview

  • Lab analysis required
  • Accurate results just 72 hours after testing begins
  • For consumers in the U.S.A
Buy Now: $115

About the Product

  • FDA-authorized saliva test
  • Customer-friendly process
  • Complete instructions included
  • Accurate results just 72 hours after testing begins
  • For consumers in the U.S.A
Buy Now: $115

How it Works

The laboratory analyzes a saliva sample provided by the consumer to determine if they were infected with COVID-19 when the sample was collected. Your test, your way: fast, safe, and accurate.

Step 1: Order test kit

Step 2: Register the kit at 1health.io/register

Step 3: Follow instructions to collect the sample

Step 4: Return the sample to the lab

Step 5: Results will be made available within 72 hours of the lab receiving the sample

Important Information

  • This test is for individual consumers only and is not available for organization/business testing through DDC

This test has not been FDA cleared or approved; the test is authorized by FDA under an Emergency Use Authorization (EUA) for use by laboratories certified under the Clinical Laboratory Improvement Amendments (CLIA) of 1988, 42 U.S.C. §263a, that meet the requirements to perform high complexity tests. 

Reach Us

Have questions or need assistance? Contact our team.

DNA Technology Park
1 DDC Way
Fairfield, OH 45014

USA: [gphone]
INT: + 1.513.881.7800

USA: [gphone_2]
INT: + 1.513.881.7800

[email protected]

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