About this item
INDICAID® COVID-19 OTC RAPID TEST 2/PK. A lateral flow immunoassay intended for the qualitative detection of SARS-CoV-2. FDA EUA Authorized for Over-the-counter use, for persons aged two years or older. Minimum order quantity applies.
- A lateral flow immunoassay intended for the qualitative detection of SARS-CoV-2
- FDA EUA Authorized for Over-the-counter use
- For persons aged two years or older
- Minimum order quantity applies
The INDICAID® COVID-19 Rapid Antigen At-Home Test is a lateral flow immunoassay intended for the qualitative detection of SARS-CoV-2. This test is authorized for non-prescription home use with self-collected direct anterior Nasal (nares) swab samples from individuals 14 years or older with symptoms of COVID-19 within the first six days of symptom onset.
This test is also intended for non-prescription home use with adult-collected anterior nasal (nares) swab samples from individuals aged two years or older with symptoms of COVID-19 within the first 6 days of symptom onset.
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- • State issued document with your organization's Federal Tax ID Number
- • State issued document with your organization's Resale Tax ID Number
- • City or County issued Business License
- • State Department of Health Services License
- • Any other ID issued by the State that includes the business name & address
* ATTN: California Customers may require additional documentation as part of the CA Health & Safety Code. Products that fall under this regulation will be placed on a mandatory 21-day hold after documentation is received. Avantor will not lift restrictions for residential shipping addresses.