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home covid test in Philippines
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home covid test in Philippines

1.2-1.5 AUD ($)

Product Details:

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home covid test in Philippines Price And Quantity

  • 1 Box
  • 1.2-1.5 AUD ($)
  • 1.20 - 1.50 AUD ($)

home covid test in Philippines Trade Information

  • USA
  • Letter of Credit (L/C) Western Union Letter of Credit at Sight (Sight L/C) Telegraphic Transfer (T/T)
  • 3 Box Per Day
  • 5-15 Days
  • Central America Middle East South America Asia Western Europe Eastern Europe North America Australia Africa
  • home covid test in Philippines.FDA EUA CE ISO GMP SFC ETC.

Product Description

If you are experiencing severe symptoms that mimic those shared by the CDC,home covid test in Philippines  such as difficulty breathing or blue lips, please seek medical attention immediately. The CDC recommends calling your healthcare provider to understand next steps after receiving a positive result for COVID-19.


Healthcare Disclaimer

Content on this site is for reference purposes only. home covid test in Philippines  Target does not represent or warrant that the nutrition, ingredient, allergen and other product information on our Web or Mobile sites are accurate or complete, since this information comes from the product manufacturers. On occasion, manufacturers may improve or change their product formulas and update their labels. We recommend that you do not rely solely on the information presented on our Web or Mobile sites and that you review the product's label or contact the manufacturer directly if you have specific product concerns or questions. If you have specific healthcare concerns or questions about the products displayed, please contact your licensed healthcare professional for advice or answers.


Legal Disclaimer

This at-home Covid-19 testing kit has not been FDA cleared or approved, but it has been authorized by FDA under an EUA. This product has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens; and, This product is 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.

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