Lead Sponsor

University of Missouri-Columbia

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

No

•1. Provision of signed and dated informed consent form
•2. Stated willingness to comply with all study procedures and availability for the duration of the study
•3. Male or female, aged 18 years and older
•4. Ability to take oral medication and be willing to adhere to the prescribed dosing regimen
•5. Self-reported cold or flu symptoms for \< 72 hours

•1. Pregnant or actively seeking to become pregnant
•2. Positive for influenza with planned treatment with oseltamivir or baloxavir
•3. Current or planned treatment with an FDA regulated drug (including those under EUA) for COVID-19
•4. Chronic liver disease (i.e. baseline liver function tests (LFTs) \> 1.5x the upper limit of normal (ULN) or established cirrhosis
•5. Chronic renal failure stage 4 or greater
•6. History of kidney stones
•7. Acute secondary bacterial infection at the time of enrollment
•8. Requiring hospitalization for any reason at the time of enrollment
•9. History of copper or iron deficiency
•10. Current prescription for quinolone antibiotics, tetracycline antibiotics, or penicillamine at the time of enrollment
•11. Allergy/intolerance to any of the active ingredients under investigation including zinc citrate, green tea, and ascorbic acid (vitamin C)
•12. Patients without decision making capacity
•13. Currently enrolled in another clinical trial for a respiratory viral infection