Department of Health and Human Services logoDepartment of Health and Human Services

Public Health Service
Food and Drug Administration

February 4, 2016

Justin Barrick
Green Garden Gold, LLC
12400 Coit Road STE 1000
Dallas, TX 75251
Re: 480747
Dear Mr. Barrick:                                                                                           
This is to advise you that the Food and Drug Administration (FDA) reviewed your website at the Internet address in January 2016 and has determined that you take orders there for the products “Regular CBD-Oil 100mg” and “CBD Strawberry Jam.” We have also reviewed your Facebook page, which provides a link to your website where products can be purchased directly. The claims on these websites establish that your “Regular CBD-Oil 100mg” and “CBD Strawberry Jam” products are drugs under section 201(g)(1)(B) of the Federal Food, Drug, and Cosmetic Act (the Act) [21 U.S.C. § 321(g)(1)(B)] because they are intended for use in the cure, mitigation, treatment, or prevention of disease. As explained further below, introducing or delivering these products for introduction into interstate commerce for such uses violates the Act. You can find the Act and FDA regulations through links on FDA’s home page at
Examples of some of the claims on your website that provide evidence that your products are intended for use as drugs include the following:
On your home page:
On the webpage titled, “ABOUT US”:
Your website also contains evidence of intended use in the form of personal testimonials recommending or describing the use of your CBD products for the cure, mitigation, treatment or prevention of disease. Examples of such testimonials include:
Further, claims made on the “About” section of your Facebook page, which includes a link to your website at where products can be purchased directly, provide additional evidence that your products are intended for use as drugs:
Your products are not generally recognized as safe and effective for the above referenced uses and, therefore, the products are “new drugs” under section 201(p) of the Act [21 U.S.C. § 321(p)]. New drugs may not be legally introduced or delivered for introduction into interstate commerce without prior approval from the FDA, as described in sections 301(d) and 505(a) of the Act [21 U.S.C. §§ 331(d), 355(a)]. FDA approves a new drug on the basis of scientific data and information demonstrating that the drug is safe and effective.
A drug is misbranded under section 502(f)(1) of the Act [21 U.S.C. § 352(f)(1)] if the drug fails to bear adequate directions for its intended use(s). “Adequate directions for use” means directions under which a layperson can use a drug safely and for the purposes for which it is intended (21 CFR 201.5). Prescription drugs, as defined in section 503(b)(1)(A) of the Act [21 U.S.C. § 353(b)(1)(A)], can only be used safely at the direction, and under the supervision, of a licensed practitioner.
Your products “Regular CBD-Oil 100mg” and “CBD Strawberry Jam” are intended for treatment of one or more diseases that are not amenable to self-diagnosis or treatment without the supervision of a licensed practitioner. Therefore, it is impossible to write adequate directions for a layperson to use your products safely for their intended purposes. Accordingly, your “Regular CBD-Oil 100mg” and “CBD Strawberry Jam” products fail to bear adequate directions for their intended uses and, therefore, the products are misbranded under section 502(f)(1) of the Act [21 U.S.C. § 352(f)(1)]. The introduction or delivery for introduction into interstate commerce of these misbranded drugs violates section 301(a) of the Act [21 U.S.C. § 331(a)].
The violations cited in this letter are not intended to be an all-inclusive statement of violations that exist in connection with your products and their labeling. You are responsible for investigating and determining the causes of the violations identified above and for preventing their recurrence or the occurrence of other violations. It is your responsibility to ensure that your firm complies with all requirements of federal law and FDA regulations.
You should take prompt action to correct the violations cited in this letter. Failure to promptly correct these violations may result in legal action without further notice, including, without limitation, seizure and/or injunction.
Within fifteen working days of receipt of this letter, please notify this office in writing of the specific steps that you have taken to correct violations. Include an explanation of each step being taken to prevent the recurrence of violations, as well as copies of related documentation. If you cannot complete corrective action within fifteen working days, state the reason for the delay and the time within which you will complete the correction.
If you need additional information or have questions concerning any products distributed through your website, please contact the FDA. You may respond in writing to Alex Brown at Food and Drug Administration, Center for Food Safety and Applied Nutrition, 5100 Paint Branch Parkway, College Park, MD 20740. If you have any questions concerning this letter, please contact Mr. Brown at
Sincerely yours,
William A. Correll
Office of Compliance
Center for Food Safety
 and Applied Nutrition
Justin Barrick

This page was posted on March 28, 2019.

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