The BinaxNOW COVID-19 Antigen Self Test is intended for non-prescription self-use and/or, as applicable for an adult lay user testing another person aged 2 years or older in a non-laboratory
FDA recommends people who get an initial negative result on an antigen test, take at least one more test 48 hours later. Take a third test, 48 hours after the second, if the second test was negative and you don’t have symptoms. Self-tests are more likely to detect the virus if you have symptoms.
Failure to follow the instructions may result in inaccurate test results. but no COVID-19 antigen was detected. If the test is negative but COVID-19-like symptoms, e.g., fever, cough, and

Note: The National Coronavirus Helpline and Easy Vaccine Access service are no longer in service. For information about COVID-19 support services and resources including information on booking a vaccination, COVID-19 vaccines, testing, and other COVID-19 services, please visit healthdirect.org.au/covid.

diagnoss of COVID -19 under Secton 564(b)(1) of the Federal Food, Drug, and Cosmetc Act, 21 U.S.C. § 360bbb- 3(b)(1), unless the decaraton ii s termnated or authorzi aton is revoked sooner. The COVID-19/Influenza A&B Antigen Test Kit is a lateral flow immunoassay for the qualitative detection of SARS-COV-2, influenza A and influenza B viral nucleoprotein antigens in nasal swabs from subjects. The symptoms of respiratory viral infection due to SARS-CoV-2 and influenza can be similar. The test is intended as an aid in diagnosis of AlQTC1. 124 919 188 349 415 253 913 245

covid 19 antigen test instructions