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INDICAID® COVID-19 Rapid Antigen At-Home Test

INDICAID® COVID-19 Rapid Antigen At-Home Test

Fast. Simple. Trusted.

Get reliable COVID-19 results at home in just 20 minutes. A rapid, non-prescription solution that delivers peace of mind and timely answers.

  • FDA EUA: 220152
  • Eligible for HSA and FSA
  • NDC code: 60008-0407-80
  • For in vitro diagnostic use only
  • Non-prescription, personal use
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INDICAID® COVID-19 Rapid Antigen At-Home Test

About

INDICAID's COVID-19 rapid antigen test is designed for easy self-administration and result interpretation without professional assistance. With a streamlined process and rapid results, it supports proactive health monitoring at home.

 

4 steps. 20 minutes. No discomfort.

INDICAID COVID-19 Antigen Rapid At-Home Test is an easy way to detect SARS-CoV-2 nucleocapsid protein antigen. The test requires just 4 simple steps and delivers results in about 20 minutes. It is noninvasive and easy to use.

 

 

 

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Hospitals, urgent care & physician clinics

Provide patients with self-testing supplies for continued at-home monitoring.

 

blue briefcase icon representing employee health and workplaces

Workplace & employee wellness

Enable employees to test at home quickly and accurately with rapid results.

 

 

Blue retail storefront icon representing retail and pharmacy

Retail & pharmacy

Offer customers fast, reliable results with convenient at-home testing.

 

 

INDICAID Omicron detection statement

PHASE Scientific continuously monitors the performance of Indicaid against emerging COVID-19 variants. To date, in-house analytical studies show no variants of concern impacting performance, including Omicron subvariants BA.4, BA.5, BQ.1, BQ1.1, XBB.1.5 and XBB.1.16.

 

View our Omicron Statement Update

 

 

It works & it's simple.

I bought the test to go to my nephew's birthday.  It was super easy to use, and totally straight forward.  Got my results done fast and was off to the party. Would totally recommend and will be using it again.

Amazon Customer

Amazon Verified Review

Specifications

 

Contents2 sterile nasal swabs (individually wrapped), 2 single-use buffer vials, 2 test devices (individually packaged), 1 quick reference guide
Tests per kit2
Speciman type

Anterior nasal swab

Time to result

20 minutes

Clinical performance
vs RT-PCR

Sensitivity: 81.7%

Specificity: 99.4%

HSA/FSA

Elibible for HSA/FSA reimbursement

Shelf life15 months from manufacture date  |  Learn More
Storage

35.6º-86ºF (2º-30ºC); do not freeze

SKUP0038

 

Intended use

The Indicaid COVID-19 rapid antigen at-home test is intended for non-prescription use with self-collected anterior nasal swab samples from individuals 14 years or older, or by an adult lay user testing individuals 2 years or older.

 

The test is authorized for:

  1. Individuals with symptoms of COVID-19 within the first 6 days of symptom onset when tested at least twice over 3 days with at least 48 hours between tests

  2. Individuals without symptoms, or with epidemiological reasons to suspect COVID-19, when tested at least 3 times over 5 days with at least 48 hours between tests

All negative results are presumptive. The Indicaid COVID-19 rapid antigen at-home test is for in vitro diagnostic use under the FDA’s Emergency Use Authorization and has not been FDA cleared or approved.

 

Frequently asked questions

 

 

The shelf-life of the INDICAID test is 15 months from the date of manufacture. The expiration date is printed on the outer box.

Yes. Data from our U.S. multicenter clinical study show similar performance for detecting the Omicron variant compared to the original COVID-19 strain.

Swab testing involves collecting upper respiratory specimens for rapid antigen or molecular testing. The CDC recognizes this method as practical, simple and efficient for generating accurate diagnostic data.

There are different kinds of tests for COVID-19. Molecular tests (also known as PCR tests) detect genetic material from the virus. Antigen tests detect proteins from the virus. Antigen tests are very specific for the virus but are not as sensitive as molecular tests. This means that a positive result is highly accurate, but a negative result does not rule out infection. Due to the lower sensitivity of antigen tests, there is a higher chance this test will give you a false negative result when you have COVID-19 than a molecular test would.

 

If your antigen test result is negative, serial testing should be performed at least twice over three days (with 48 hours between tests) for symptomatic individuals and three times over five days (with at least 48 hours between tests) for asymptomatic individuals. You may need to purchase additional tests to perform this serial (repeat) testing. All negative results are presumptive.

 

Discuss with your healthcare provider whether a molecular test would help with your care, and when you should discontinue home isolation if necessary. If a molecular test is not available, the CDC recommends that you should stay home.

 

Refer to the CDC website for most updated guidelines: https://www.cdc.gov/coronavirus/2019-ncov/your-health/isolation.html

No. Antigen tests are less sensitive than molecular tests, which detect viral nucleic acids. Negative results should be considered presumptive and may be confirmed with a molecular test if needed. Always interpret results alongside recent exposures, medical history and symptoms consistent with COVID-19.

Several factors can affect accuracy:

 

• The test does not distinguish between SARS-CoV and SARS-CoV-2, which may produce a false positive.

 

• Testing too early or too late may yield a false negative, as antigen levels decline over time.

 

• Results from patients with symptoms beyond 5 days may require confirmation with a molecular test.

 

• Improper handling of the kit may cause imprecise results.
 

• When results are unclear, consult your healthcare provider for evaluation and next steps.

A negative test result means that proteins from the virus that causes COVID-19 were not found in your sample, all negative results are presumptive. However, it is possible for this test to give a negative result that is incorrect (false-negative) in some people with COVID-19. Your healthcare provider will consider the test result together with all other aspects of your medical history (such as symptoms, possible exposures, and geographical location of places you have recently traveled) in deciding how to care for you.

 

Serial testing should be performed in individuals with negative results at least twice over three days (with 48 hours between tests) for symptomatic individuals and three times over five days (with at least 48 hours between tests) for asymptomatic individuals. You may need to purchase additional tests to perform this serial (repeat) testing.

A positive test result means that proteins from the virus that causes COVID-19 were found in your sample. This means that it is likely that you have COVID-19, even if you do not have any symptoms. There is also a very small chance that this test can give a positive result that is incorrect (a false-positive), particularly when used in a population without many cases of COVID-19. Your healthcare provider will discuss the next steps with you and how to best care for you based on your medical history and symptoms.

 

The INDICAID COVID-19 Rapid Antigen Test is for diagnosis only and is safe to use, with no long-term impact on human health.

 

Potential risks include:

Possible discomfort or other complications that can happen during sample collection.

 

Possible incorrect test result (see below for more information).

 

Potential benefits include:

The results, along with other information, can help your healthcare provider make informed recommendations about your care.

 

The results of this test may help limit the spread of COVID-19 to your family and those you come in contact with.

 

For detailed information see the “Warnings, Precautions, and Safety Information” section of the Instructions For Use (IFU).

This test can be administered with no equipment or training needed. The test has high sensitivity and can detect lower viral load samples against competitive products. This test has been granted Emergency Use Authorization (EUA) by the United States Food and Drug Administration.

The INDICAID COVID-19 Rapid Antigen Test is a lateral flow immunoassay designed for the qualitative detection of SARS-CoV-2 antigens. Antigen tests are designed to detect proteins from the virus that causes COVID-19 through swab specimens taken from the patient’s nose.

 

INDICAID OTC Rapid Antigen Test Instruction Guide

 

 


Step 1:
Collect sample 
Tilt your head back slightly. Insert the swab about 1 inch into one nostril. Rub the swab against the wall of the nostril in a circular motion 4 times. Repeat in the other nostril.

Step 2: Insert swab & stir
Remove the vial cap. Place the swab into the buffer solution and stir 20 times. Discard the swab and secure the cap.

Step 3: Apply sample
Hold the vial vertically. Add 3 drops of solution into the sample well (S) of the test device.

Step 4: Read results
Wait 20 minutes, then read the results. Do not read after 25 minutes.
 

Reading test results

 

You can also find the results diagram in the Instructions for Use (IFU) inside your Indicaid OTC box.

 

Report your test result(s) at MakeMyTestCount.org – voluntary, anonymous reporting helps public health teams track COVID-19 spread in your community and nationwide.

 

Questions? Visit our FAQ’s or contact customer support.

 
Test result interpretation

 

CT indicatorResult
A line appears in regions (C) and (T)Positive
A line appears in region (C)Negative
No line appears in region (C)Invalid

 

Positive
If the control (C) line and the test (T) line are visible, the test is positive. Any faint visible red colored test (T) line with the control (C) line should be read as positive. No serial testing is required if you get a positive result at any point.

 

Negative
If the control line (C) is visible, but the test (T) line is NOT visible, the test is negative.

 

To increase the chance the negative result for COVID-19 is accurate, you should:

  • Test again in 48 hours if the individual has symptoms on the first day of testing.
  • Test 2 more times at least 48 hours apart if the individual does not have symptoms on the first day of testing.

 

Invalid
No red-colored line next to the "C" means the test is invalid. Re-test with a new swab and a new test device.

 

Contact Sales & Customer Service

Email Sales

ussales@phasesci.com

Call Sales

+1 (657) 233-5880

Customer Service

+1 (657) 296-6106