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WARNING LETTER
•Santhigram Kerala Ayurvedic Co. of U.S., Inc.•May 24, 2022

Santhigram Kerala Ayurvedic Co. of U.S., Inc. – FDA Warning Letter, May 24, 2022

Record Details

The FDA issued a Warning Letter to Santhigram, LLC, following a March 2022 review of their website (santhigram.us) and social media (Facebook, Instagram). The FDA observed that Santhigram takes orders for various ayurvedic products, including "Smokers Kit/Respiratory Care Kit," "Immunocare Kit," "Dadimadi Ghrutham," "Dasamoolarishtam," "Maha Tiktaka Ghrutham," "Padoladi Ghrutha," "Ashwagandha," "Triphala," "Garlic," "Eladi Taila," "Jathyadi Ghrutham," and "Jatyadi Keram."

The "Smokers Kit/Respiratory Care Kit" and "Immunocare Kit" are specifically cited for claims intended to mitigate, prevent, treat, diagnose, or cure COVID-19. The FDA determined that claims on Santhigram's websites establish these products as unapproved new drugs, violating sections 505(a) and 301(d) of the FD&C Act (21 U.S.C. 355(a) and 331(d)). The products are considered "drugs" under section 201(g)(1) (21 U.S.C. 321(g)(1)) due to their intended use in disease diagnosis,

Company
Santhigram Kerala Ayurvedic Co. of U.S., Inc.
Inspection date
May 24, 2022
Product type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Carolyn E. Becker
View Company Profile

ID · 602f67c7-b654-4859-b3a8-328acabde8d1

Violation Codes4
21.U.S.C. 355(a)21 U.S.C. 331(d)21 U.S.C. 321(g)(1)21 U.S.C. 321(p)

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