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WARNING LETTER
•Ora, Inc.•October 31, 2019

Ora, Inc. – FDA Warning Letter, Oct 31, 2019

Record Details

On November 22, 2019, the FDA issued a Warning Letter to Sunflora, LLC, following a review of their websites (sunflora.org, cbdrx4u.com) and social media (instagram.com/yourcbdstoreofficial/) from July to October 2019. The letter identified multiple violations related to the marketing and sale of products containing cannabidiol (CBD).

The FDA determined that Sunflora's "Sunmed Tincture," "Sunmed Water Soluble," "Sunflora CBD Daytime Ageless Moisturizer," "Sunflora CBD Nighttime Ageless Serum," and "Sunmed Topical Relief Cream" are unapproved new drugs, sold in violation of sections 505(a) and 301(d) of the FD&C Act, and are misbranded drugs under section 502(f)(1) due to inadequate directions for use. Promotional claims on their websites established drug intended use, such as treating pain, anxiety, and inflammation.

Additionally, "SunMed Bacon Dog Treats," "SunMed Pet Bark Bits Beef," "SunMed Dog Lamb Bits," and "SunMed Pet Tincture" were deemed unapproved new animal drugs, unsafe under section 512(a) and adulterated under section 501(a)(5) of the FD&C Act. Claims indicated intended use for animal health issues like anxiety and pain.

Company
Ora, Inc.
Inspection date
October 31, 2019
Product type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Donald D. Ashley (Director)
  • Eric M. Nelson (Director - Division of Compliance)
  • William A. Correll (Director)
View Company Profile

ID · 366ddf1b-3c3b-43b6-b646-1c16ab6ac3c2

Violation Codes10
21.U.S.C. 355(a)21 U.S.C. 331(d)21 U.S.C. 352(f)(1)21 U.S.C. 360b(a)21 U.S.C. 351(a)(5)21 U.S.C. 342(a)(2)(C)(i)21 U.S.C. 331(ll)21 U.S.C. 321(ff)21 U.S.C. 321(ff)(3)(B)(i)21 U.S.C. 321(ff)(3)(B)(ii)

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