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COVID-19 Active Infection Testing Information and Resources

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COVID-19, Flu & RSV Active Infection Test

Who should be tested?

Individuals infected with COVID-19, influenza A/B or RSV often experience similar symptoms of cough, fever, and a runny and/or stuffy nose. Because flu and COVID-19 especially share so many similar symptoms, the CDC advises that patients may need testing to confirm a diagnosis. Patients may also be considered for testing if they have come into contact with someone they know who is infected by the coronavirus or meet criteria established by the CDC.

Sample

Short nasal swab

Where are samples collected?

• At a healthcare provider office, hospital, or other designated testing location under supervision of a healthcare provider.

Getting Tested

Patients can visit a physician's office for testing.

Labcorp Test Number

Physicians have test options:

2019 Novel Coronavirus (COVID-19), NAA 139900

2019 Novel Coronavirus (COVID-19) with Influenza A, Influenza B and Respiratory Syncytial Virus, NAA 140140

2019 Novel Coronavirus (COVID-19) with Influenza A and Influenza B, NAA 140147

Influenza A, Influenza B and Respiratory Syncytial Virus, NAA 140163

Influenza A and Influenza B, NAA 140165

2019 Novel Coronavirus (COVID-19) with Respiratory Syncytial Virus, NAA 140172

Receiving Results

• As of November 17, 2020, the current average time to deliver results for COVID-19, Flu & RSV combined testing is 1-3 days from the date of specimen pickup.
• Delivered to the ordering physician's EMR or Labcorp Link

Additional Information

• Labcorp COVID-19 Specimen Collection Guide (Illustrated)
• COVID-19 Direct Observed Patient Specimen Collection
• SARS-CoV-2 Specimen Collection Supplies Q&A
• COVID-19 Nucleic Acid Amplification Nasal Swab (Anterior Nares) Collection for Healthcare Providers
• COVID-19 PCR Testing Specimen Collection Grid
• COVID-19 RT-PCR Test (anterior nares) specimen collection instructions (foam swab)

• FDA Emergency Use Authorization Documents
  • LabCorp COVID-19 RT-PCR Test Fact Sheet for Providers
  • LabCorp COVID-19 RT-PCR Test EUA Summary

Labcorp’s COVID-19 PCR test has not been FDA cleared or approved, has been authorized by FDA under an Emergency Use Authorization (EUA), and has been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens. The 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 Act, 21 U.S.C. § 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner.

COVID-19 Information and Resources

Have a Question?

Find answers to the most common Provider and Payer questions about COVID-19 testing.

FIND ANSWERS

Helpful COVID-19 Resources

• Which Test is Right for Your Patients and Members? (Test Options Infographic)
• Telemedicine Toolkit
• Video Resources
• LabCorp At Home COVID-19 Test Collection Service
• Learn More: U.S. Department of Health & Human Services' Combat COVID website

More Information

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