COVID-19 SELF TESTING
Designed for the ultimate convenience, for self-testing anywhere or anytime.
OHC COVID-19 Antigen Self Test
Convenient, Reliable, and Easy-To-Use
The OHC COVID-19 Antigen Self Test is a lateral flow assay intended for the qualitative detection of COVID-19 in nasal swab samples collected from individuals within 7 days of the onset of symptoms or infected individuals without symptoms.
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Using the easy nasal swab test, you can self-collect samples with highly accurate and reliable results you can expect in just 15 minutes.
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Feel safe and confident about whether or not you have symptoms of COVID-19. The OHC COVID-19 Antigen Self Test detects both Omicron and Delta variants.
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Children starting at the age of 14 can self test.
Children from ages 2 to 13 require the help of an adult.
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*Clinical Data shows, OHC COVID-19 Antigen Self Test showed a relative sensitivity of 91% ( 95% CI: 82.8 to 95.6%)
at high viral loads (less than a cycle threshold (Ct)-value of 30) and relative specificity of 99% (95% CI: 95.2 to 99.6%).
Kit Contents
Test Cassette
Nasal Swab
Buffer Tube
Filter Cap
Kit Box
Instructions for Use
Use the buttons below to open a downloadable PDF copy of the Quick Instructions for Use (QRI) in English or Spanish.
For healthcare professionals,
use the buttons below to open a downloadable PDF copy of the Healthcare Provider IFU (Instructions for Use) and Fact Sheet for Healthcare Professionals.
BEFORE GETTING STARTED: CHECK YOUR KIT EXPIRATION DATE
On August 19, 2022, the FDA granted a shelf-life extension for OHC COVID-19 Antigen Self Test
from 8 months to 12 months. Confirm your expiration date by referring to the lot number on the box,
demonstrated on the image to the right:
Refer to the image on the right for the location of the lot number on each OHC Covid-19 Antigen
Self Test kit box.
Once you locate the lot number, follow this link:
**To check your expiration date, use this link**
https://www.fda.gov/media/161358/download?attachment
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The image below is from the U.S. Food & Drug Administration webpage in regards to OSANG LLC's Covid-19 Antigen Self Test. Please click the link provided above and review the information to determine whether you may use your test.
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1. Bring test kit to room temperature (15-30oC / 59-86oF). **Before washing your hands, please prepare by blowing your nose.**
2. Wash your hands with soap and water, or use hand sanitizer before performing the test. Make sure you rinse thoroughly and your hands are dry before starting.
3. Check test expiration date on the back of the foil. Do not use if the expiry date has been passed.
4. Open the pouch and remove the test device from the foil pouch. Ensure the desiccant contains only white and yellow beads.
Note: If green beads are present, use a new test device.
5. Place the test device on a flat surface
Prepare to Perform the Test
1. Bring test kit to room temperature (15-30°C / 59-86°F).
**Before washing your hands, please prepare by blowing your nose.**
2. Wash your hands with soap and water, or use hand sanitizer before performing the test. Make sure you rinse thoroughly and your hands are dry before starting.
3. Check test expiration date on the back of the foil. Do not use if the expiry date has been passed.
4. Open the pouch and remove the test device from the foil pouch. Ensure the desiccant contains only white and yellow beads.
Note: If green beads are present, use a new test device.
5. Place the test device on a flat surface
Follow the Seven Steps
STEP 1: OPEN TUBE & PLACE TUBE IN TUBE HOLDER
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Open the pouch that contains the extraction buffer tube & filter cap.
Open the seal of the tube carefully without spilling the liquid inside the tube.
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Punch a hole in the box to hold the tube.
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If any liquid spills, do not use the tube.
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READ & INTERPRET THE RESULTS
WARNING:
Inaccurate test interpretations may occur if results are read before 15 minutes or after 20 minutes.
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Look at the result window and locate the letters C and T on the side of the window.
A pink/purple line should always appear at the C position; this is a control line and signals that the test is working properly.
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Report your test result(s) at MakeMyTestCount.Org – this voluntary and anonymous reporting helps public health teams understand COVID-19 spread in your area and across the country and informs public health decisions.
Easy-To-Read Results
Large sample loading port
Large results window
Thick results lines
POSITIVE RESULT
If the Control (C) line and the Test (T) line are visible, the test is positive. Any faint visible pink/purple test (T)
line with the control line (C) should be read as positive.
You do not need to perform repeated testing if you have a positive result at any time.
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A positive test result means that the virus that causes COVID-19 was detected in your sample and it is likely you have COVID-19 and are contagious. Please contact your doctor/primary care physician or your local health authority immediately and adhere to the local guidelines regarding self-isolation.
There is a very small chance that this test can give a positive result that is incorrect (a false positive).
NEGATIVE RESULT
To increase the chance that the negative result for COVID-19 is accurate, you should:
- Test again in 48 hours if you have symptoms on the first day of testing.
- Test 2 more times at least 48 hours apart if you do not have symptoms on the first day of testing.
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A negative test result indicates that the virus that causes COVID-19 was not detected in your sample. A negative result is presumptive, meaning it is not certain that you do not have COVID-19. You may still have COVID-19 and you may still be contagious. There is a higher chance of false negative results with antigen tests compared to laboratory-based tests, such as PCR. If you test negative and continue to experience COVID-19 like symptoms (e.g., fever, cough, and/or shortness of breath) you should seek follow up care with your healthcare provider.
INVALID RESULT
If a control (C) line is not visible, the test is invalid. Re-test with a new swab and new test device.
Trusted & Proven
Rapid self testing
anytime, anywhere
Quality manufacturing
at significant scale
Trusted and tested
FDA approved
NIH RADx graduate
NIH ITAP graduate
OHC products trusted in markets across the globe
Detecting All Mutations
The OHC Ag Rapid Test's Diagnosis Test's anti-body design was validated by the United States NIH (National Institution of Health) and the ITAP (Independent Test Assessment Program) with outstanding recognition rates for all mutations.
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Through the United States NIH and ITAP we were able to test and confirm detection of the SARS-CoV-2 despite any previous or current MOH VOC which includes Omicron BA.4 and BA.5.
Performance
91% relative sensitivity
99% relative specificity
The OHC COVID-19 Self Test has not been FDA cleared or approved; but has been authorized by FDA under an Emergency Use Authorization.
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*Clinical Data shows, OHC COVID-19 Antigen Self Test showed a relative sensitivity of 91% (95% Cl:82.8 to 96.6%) at high viral loads (less than a cycle threshold (Ct-valve of 30) and relative specificity of 99% (95% Cl: 95.2 to 99.6%)
Ideal For Any Testing Scenario
Know Before You Go...
On a Trip
Test before and after travelling to reduce transmission.
To Work
Quick and easy way to protect coworkers.
To School
Approved for use ages 2 and up.
To Vulnerable Sectors
Non-invasive and easy-to-use for the vulnerable.