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COVID-19 Rapid Antigen Home Test (2-Pack)

Celltrion DiaTrust At-Home COVID-19 Rapid Antigen Test (2-Pack)
  • Two (2) rapid antigen (Ag) tests for COVID-19
  • Results in 15 minutes
  • Reimbursable by insurance *
  • Painless and easy swab
  • Free shipping
  • Free shipping on orders over $150
Collection Method: Shallow Nasal Swab

Out of stock

* COVID Testing Tip:

Health insurers are now required to cover at-home tests at up to $12 per test and up to 8 tests per person every month. Order your test and take advantage of these savings by filing for reimbursement directly with your insurance company.

Manufacturer details : Celltrion DiaTrust™

DiaTrust COVID-19 Ag Home Test Fact Sheet for HCP
DiaTrust COVID-19 Ag Home Test IFU
DiaTrust COVID-19 Ag Home Test IFU for HCP
DiaTrust COVID-19 Ag Home Test Box Labels

Sample Type Direct Mid-Turbinate Swab Samples
Sample-to-answer-time 15 mins
FDA Status For use under the emergency use authorization (EUA) only
Authorized Setting Non-prescription home use (OTC)


  • This product has not been FDA cleared or approved; but has been authorized by FDA under an EUA;
  • This product has been authorized only for the detection of proteins from SARS- CoV-2, not for any other viruses or pathogens; and,
  • The emergency use of this product 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 declaration is terminated or authorization is revoked sooner.

Testing for COVID-19

Celltrion DiaTrust™ COVID-19 Ag Home Test is a lateral flow immunoassay intended for the qualitative detection of nucleocapsid protein and receptor binding domain (RBD) of the SARS-CoV-2 spike proteins in mid-turbinate swabs from the SARS-CoV-2.

Due to FDA Guidelines and Supply Chain Demands All Orders for this Product are NON-Cancellable and NON-Returnable.

The test collection kit uses a non-invasive self-collected shallow nasal swab sample. Self-collection of shallow nasal swab is painless and reduces the risk of spreading COVID-19 to the public and to healthcare providers compared to collecting NP swabs in the office or hospital.

Test results will be available in as little as 15 minutes after sample collection.

Who should be tested and why?

To limit the spread of the COVID-19 epidemic in the United States, it is important to test at-risk individuals in the community. Infected individuals can then isolate at home, reducing the likelihood that they will infect others. In addition, contacts of infected individuals can themselves be tested, and if infected, stay home as well.

There are many reasons for ordering a test for COVID-19:

  • Symptoms of possible COVID-19 infection (see *** below)
  • Exposure to a lab-confirmed COVID-19 infected individual
  • Travel overseas in places with large numbers of COVID-19 infected individuals
  • Employment in industries such as grocery stores, pharmacies, nursing homes, transportation, delivery services, warehouse/distribution, and banking
  • Have a chronic condition such as chronic lung disease (asthma/emphysema/COPD), diabetes mellitus, heart disease, chronic kidney or liver disease, cancer, immunocompromised conditions, or receiving immunosuppressive drugs

*** If you have any of the following emergency warning signs and symptoms of a serious COVID-19 infection (difficulty breathing or shortness of breath, persistent pain or pressure in the chest, new confusion or inability to arouse, bluish lips or face), please do NOT order a test for COVID-19. Please instead call your health care provider immediately, and failing to reach them, go to the nearest emergency room or dial 911.

Included: 1 At-Home Rapid Covid-19 Ag Test kit

While there are multiple vaccines for COVID-19, rapid diagnosis remains pivotal to minimizing transmission.

Insurance Reimbursement

How to apply for reimbursement with your insurance provider?

As of January 15, 2022, your insurance provider must reimburse 8 total tests per member for personal use in a 30-day period. For test kits that come in packs of 2, each test counts towards your total limit of 8 (4 two-packs would count towards your limit of 8 tests). To receive reimbursement, make sure to save your myLAB Box receipt and note the UPC code from the test kit packaging. Follow the steps provided by your insurance provider to submit a claim. Please find links below to many common insurance providers for your convenience:

Blue Cross Blue Shield


Anthem, Inc.


CVS Caremark

Cigna Health

Molina Healthcare, Inc.

Independence Health Group

Doctor with stethoscope

Fully Lab-certified

myLAB Box works only with the best laboratories and health experts to ensure your tests results meet nationwide standards and are as accurate as tests done in a clinic or a doctor’s office.

The laboratories we work with are certified CAP and CLIA high complexity testing organizations at the forefront of diagnostic testing. HIPAA web security protocols protect your data.

  • Pay with FSA / HSA cards
  • CDC Listed
  • Labs CAP & CLIA Certified

Fast, Easy & Private

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Step 1

Order online on your mobile, tablet or PC

Contents of myLAB Box test kit

Step 2

Collect & mail in your sample in 5 minutes

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Step 3

Get lab-certified results online in 1-5 days

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Non-invasive shallow nasal swab test to screen for the COVID-19 virus. Can detect an infection in as little as 1-2 days from infection in as little as 48 hours. FDA authorized.

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myLAB Box offers individuals with laboratory services for wellness monitoring. All tests are validated by myLAB Box clinical laboratory affiliates. Results are comparable to samples collected in a physician’s office or clinical laboratory. Tests used in myLAB Box kits have been developed and performance characteristics determined by myLAB Box clinical laboratory affiliates. These tests are used for clinical purposes only. They should not be regarded as investigational or for research. myLAB Box clinical laboratory affiliates are regulated under the Clinical Laboratory Improvement Act (CLIA) of 1988 as qualified to perform high complexity clinical testing and follow the guidelines of the College of American Pathologists (CAP). The tests, and services are not intended to diagnose, treat, or cure disease. All information given as to the use of the tests is provided for educational purposes only and is not intended to be a substitute for a physician’s consultation. In the event you test positive and have a telemedicine consultation with your ordering physician (licensed in your state) or his/her designate, all additional health care instructions, ongoing care, and possible need for prescriptions if not provided will be your responsibility to obtain from your own healthcare provider. Copies of your test results will be made available for you to share with your healthcare provider. If you do not have a health care provider, you can search for one on the internet, get recommendations from family or friends, call your local county medical society or local hospital physician referral service, or seek care from a local urgent care facility.

If you are diagnosed with COVID-19, it is best to self isolate and to speak with a healthcare provider for further instructions. If you think you have a medical emergency, call 911 or proceed to the closest emergency room.

Tests for COVID-19 have been authorized by the FDA under an EUA for use by authorized laboratories. These tests are 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.

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