Exp Date: January 2025
(Rapid Results In 10 Minutes)
The QuickVue At-Home OTC COVID-19 Test by Quidel Corporation is a rapid test that is defined as a lateral flow assay intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 also known as Covid 19. The Antigen test is authorized by the FDA as a non-prescription home use with self collection direct anterior nasal (nares) swab samples from individuals aged 14 years or older with symptoms of COVID-19 within the first six days of symptom onset. This Quickvue At Home Antigen Test 2pk test is also authorized for non-prescription home use with adult-collected anterior nasal swab samples from individuals aged 2 years or older with symptoms of COVID-19 within the first six days of symptom onset. The manufacturer of the test is Quidel Corporation located within the United States.
Peach Medicalis is an authorized distributor of Quidel products. Purchase Quickvue Self Test Online with confidence.
Please call us at 1-877-597-3224 or e-mail us email@example.com for wholesale pricing on Quickvue Covid Tests. We are more than happy to provide references in theatre, government, banking, education, fortune 500 companies, and more. Over 50,000+ orders of test kits sold over the past year.
In a clinical study, the QuickVue At-Home OTC COVID-19 Test identified positive cases 83.5% of the time, and identified negative cases 99.2% of the time (83.5% PPA, and 99.2% NPA, respectively), when compared to PCR Test. For more information on comparing Antigen Tests and PCR test, please check out our recent article.
The Quickvue At-Home OTC COVID-19 test can accurately detect the Omicron variant (among others) of the Sars-CoV-2, the potentially deadly virus that can lead to COVID-19.
Please note that all Peach Medical shipments do not require signature upon delivery. Since most test kits should be stored between 35.6 and 86 degrees F range, we strongly recommend that you track your order and anticipate its delivery. However, if the test is stored outside the temperature range for a relatively short period of time – for a couple of hours up to a day or two – it will be fine to use as long as the test and it’s components are used at room temperature. Peach Medical is not responsible if the test kits are left outside in extreme temperatures for longer than the recommended time frame after delivery.
The QuickVue At-Home OTC COVID-19 Test is a type of test called an antigen test. Antigen tests are designed to detect proteins from the virus that causes COVID-19, in anterior nasal swabs.
The QuickVue At-Home OTC COVID-19 Test is testing for the presence or absence of nucleocapsid antigens from SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2), which causes the disease Coronavirus Disease 2019 (COVID-19).This is not an antibody test. For more information on the difference between an antigen test and a pcr test visit our blog.
This test is authorized for symptomatic or asymptomatic individuals aged 2+ (ages 2–13 require adult-assisted collection, whereas ages 14+ can self-collect).
not intended for individuals experiencing severe COVID-19 symptoms, who should seek emergency medical care right away.
The QuickVue At-Home OTC COVID-19 Test is intended to be used for serial testing of asymptomatic individuals or used twice by the same individual over two or three days with at least 24 hours (and no more than 48 hours) between tests or once by symptomatic individuals within the first six days of symptom onset. By testing more frequently, you may detect COVID-19 more quickly and reduce the spread of infection.
The test is available for at-home use without a prescription. Please consult with your specific health insurance to make sure the test can be reimbursed. Information on insurance company coverage can be found on the CMS website.
Everything you need to collect and test your sample and understand your results:
Care support is available if needed
Only a pink line about half of a centimeter below the blue control line should be considered a positive result. A pink line bordering the black label with the arrows, a vertical pink line, or a faint grey line next to the blue control line is not considered a positive test line and should not be called a positive result.
The test is intended for the individuals with or without symptoms or other epidemiological reasons to suspect COVID-19.
Individuals who test positive with the QuickVue At-Home OTC COVID-19 Test should self-isolate and seek follow-up care with their physician or healthcare provider as additional testing may be necessary.
The QuickVue At-Home OTC COVID-19 Test meets all accuracy requirements as defined by the FDA. The performance was measured during a clinical study that compared the QuickVue At-Home OTC COVID-19 Test results to an FDA Emergency Use Authorized high sensitivity PCR (molecular) test. Positive Percent Agreement (PPA) and Negative Percent Agreement (NPA) for both symptomatic and asymptomatic individuals were 83.5% and 99.2%, respectively.This product has not been FDA cleared or approved but has been authorized by FDA under an Emergency Use Authorization (EUA). This product has been authorized only for the detection of proteins from SARS- CoV-2, not for any other viruses or pathogens. 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.
There are two tests (as well as two swabs and reagents) in each box.
Test cost may be eligible for reimbursement with health insurance. HSA and FSA purchases are permitted. Once your order is complete, you can work with your health insurance provider on reimbursement. Before purchasing, always check with your insurance provider to confirm benefit coverage.
The QuickVue At-Home OTC COVID-19 Test is intended for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 from individuals within 6-days of symptom onset or individuals without symptoms or other epidemiological reasons to suspect COVID-19 infection when tested twice over three days with at least 24 hours (and no more than 48 hours) between tests.
This product has not been FDA cleared or approved; but has been authorized by FDA under an Emergency Use Authorization (EUA) for the Public Health Emergency This product has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens. 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.
For more information on EUAs please visit the FDA's Website
For the most up to date information on COVID-19, please visit the CDC's Website
Items are shipped Monday - Friday from our warehouse. 1-2 Day Processing Time.
For B2B accounts, please contact us at firstname.lastname@example.org for urgent orders requests.
Please feel free to contact email@example.com if you have any questions.
At Peach Medical we use UPS (most orders ship via UPS but some may ship via USPS) as our logistic and Shipping partners. We currently offer the following services:
UPS Next Day Air
UPS 2nd Day Air
UPS Ground (3-5 Day Delivery)
Our system updates clients every evening with tracking numbers for their orders. This will be sent via e-mail with an additional copy of your receipt.
Please verify your address when ordering, we are unable to fix an incorrect shipping address on an order once it is in transit. If your order is in transit with an incorrect address, please reach out to your carrier to reroute the package. Peach Medical is not able to have packages rerouted or contact the carrier on your behalf.
Refunds will not be issued for packages that were shipped to an incorrect address but it may be possible for a replacement package to be sent, please contact the customer service team to see if you are eligible.
All sales are final. If items are found defective, the customer has 7 Business Days to request a return label. We are not responsible for any delays caused by shipping companies, ie: UPS, Fedex, DHL, Freight.
If a customer chooses a 3rd party receiver who is not the purchaser, Peach Medical is not responsible for any goods once it leaves our warehouse and when tracking is provided. I.e Gifts, International Shipping Services.
Note: If Peach Medical has not shipped your item within 7 business days, cancellations will be honored.