Search Results for: CBD

CBD Brand Mendi Partners With Jars Cannabis and Pro Skateboarder Leo Baker on Volunteer ‘Build And Ride Day’

Volunteer event WAKE-N-SKATE at Bishop DIY Skatepark will feature the build of new skateboard features and a Q&A discussion on CBD/THC and cannabis in the skate community.

 

MICHIGAN: Developed and created by professional athletes, all-natural recovery cannabis brand MENDI has added leading Michigan-owned cannabis retailer JARS Cannabis as its newest retail partner for 2021. To kick off this partnership, the brands, along with professional skateboarder and MENDI brand ambassador Leo Baker (they/them), will come together for an exciting one-day event to support Community Push, a  Detroit non-profit  that bridges the gap between skateboarders and their communities. WAKE-N-SKATE is a true philanthropic community event and will be held at Bishop DIY Skatepark in Detroit. The event will include a build of new features exclusive to the park, park-wide clean-up, and an intimate discussion with Leo Baker. Additionally, JARS will donate $5,000 to support Community Push and its initiatives throughout Detroit. A 20% off coupon will be provided to those in attendance to use towards their next purchase at JARS Cannabis. 

“We’re thrilled to be partnering with JARS Cannabis and rolling out Mendi into the Michigan market,” says MENDI co-founder and CEO, Rachael Rapinoe. “This is a very exciting step for our brand, and we’re grateful for their support in helping expand our retail footprint. There’s natural alignment with JARS in thinking creatively to amplify this partnership while also giving back to the community of Detroit with our ambassador, Leo Baker.”

Who: Professional skateboarder Leo Baker
When: Friday, October 22, 2-6PM EST
Where: Bishop DIY Skatepark, 6017 Grand River Avenue., Detroit, MI, 48208

Baker, a seven-time X Games medalist, left the inaugural U.S. Women’s Olympic Skateboard team in 2020 in order to publicly change their name to Leo and focus on mental health and their gender identity journey. Their inspiring story was brought into the public eye when they were featured in a Miley Cyrus video in 2019 and became the first-ever openly trans person to be represented in a video game (Tony Hawk Pro Skater). Since then, the professional athlete has focused on increasing non-binary visibility and introducing trans inclusivity to a predominantly straight, cis-male skate industry while partnering with brands like MENDI, who are committed to bringing representation and equality to the world of sports and beyond.

“Overall Mendi CBD has been a benefit in every part of my life, when I’m skating, meditating, or just getting into some music. Discovering Mendi has been super helpful for me in maximizing my recovery and spending more time on my skateboard. I am looking forward to being on the ground with other skaters, especially in Detroit, and creating more safe and sick spaces to skate.”

WSLCB Prohibits Conversion of CBD to Delta-8 THC; Purchase or Sale of Hemp-derived Delta-8 THC

To:               Cannabis Industry Members

From:           Chandra Brady, Enforcement and Education Div. Director

Subject:      Prohibited: conversion of CBD to delta-8 THC; purchase or sale of hemp-derived delta-8 THC

Enforcement Bulletin 21-03

This bulletin is offered in response to stakeholders who have requested additional guidance regarding delta-8 THC following the release of LCB Policy Statement #PS21-01 on April 28, 2021.

Policy Statement # PS21-01, Tetrahydrocannabinol (THC) compounds other than delta-9 and the conversion of CBD, hemp, or both to delta-8 THC, delta-9

THC, or any other cannabis compound that is not currently identified or defined in the Revised Code of Washington (RCW), the Washington Administrative Code (WAC), or both.

Policy Statement #PS21-01 referenced that under RCW 69.50.204, delta-8 THC and synthetic equivalents are Schedule 1 controlled substances. Under current law, marijuana license holders are not allowed to produce or process delta-8 THC. Likewise, marijuana licensees may not buy or sell hemp-derived delta-8 THC. Engaging in this activity is a violation of the Uniform Controlled Substances Act (RCW 69.50.401).

What does this mean for licensees?

  • Processors are not allowed to convert CBD or hemp into delta-8 THC.
  • Processors are not allowed to buy or sell delta-8 THC products not legally produced.
  • Retailers should not knowingly purchase products from processors which contain delta-8 THC converted from CBD. Nor should retailers sell such products to consumers. 

How will WSLCB Enforcement and Education staff approach this in the field?

The Enforcement and Education team will approach this from an education-first perspective so we can help licensees achieve compliance. Our team has several tools to use to help; communication, basic education, administrative holds, warnings, notices to correct. If we identify licensees who are knowingly and intentionally violating rules and law or licensees who do not demonstrate a desire to achieve compliance, we will take appropriate enforcement action.

Are there any exceptions?

There are no exceptions.

If you have any questions, please contact your assigned compliance consultant or enforcement officer.

Curt’s Cannabis Corner: CBD For Epilepsy

Welcome to Season 2, Episode 2 of Curt’s Cannabis Corner, an education series from technical writer Curt Robbins at Higher Learning LV and MJNews Network intended for cannabis and hemp professionalsand the enterprise organizations that employ themwho wish to gain a better understanding of the nuanced biochemistry, volatile business environment, and detailed regulatory oversight of this newly legal herb. 

This week, readers learn about the recent scientific investigative work of Dr. Nicolas Schlienz, a research scientist and clinical psychologist. Schlienz was recently appointed to the position of Research Director for Realm of Caring, a pioneering non-profit cannabinoid research organization based in Colorado Springs with ties to the popular vertically integrated brand Charlotte’s Web.  


CURT’S

CANNABIS

CORNER 

CBD

For

Epilepsy

 

By Curt Robbins

 


 

Dr. Nicolas Schlienz & CBD for Epilepsy

In July 2021, Schlienz coauthored a study entitled “Cross-sectional and Longitudinal Evaluation of Cannabinoid (CBD) Product Use and Health Among People with Epilepsy” that was published in the peer-reviewed journal Epilepsy & Behavior

“This study represents a refreshing collaboration of scientists, clinicians, patients, and advocates,” said Jay Salpekar, MD, Associate Professor of Psychiatry and Neurology at Johns Hopkins University. Salpekar said that the study affirms that “cannabinoid products have value in the treatment of epilepsyas well as associated neuropsychiatric conditions.”

The study observed that cannabis “and select chemicals found in the cannabis plant have received significant clinical attention as evidence accumulates suggesting potential utility for varied health conditions.” It noted that multiple recent studies have “demonstrated the safety and efficacy of CBD in the reduction of seizures for several specific epilepsy syndromes.”

The study stated that the efficacy of CBD for those who suffer epilepsy goes beyond seizure control. “CBD products may prove valuable for their effects on psychosocial function and psychiatric health,” stating that a variety of behavior issues, including psychiatric disorders, are “overrepresented among people with epilepsy.”   

This study is of importance because it was conducted on human participants, not in test tubes or on animal subjects. Participants were “predominantly Caucasian (74 percent) with a roughly even split by gender (55 percent female), an average of 21 years old (51 percent were under 18), and the majority (90 percent) had no history of non-medicinal (‘recreational’) cannabis use.” 

93 percent of the study participants reported epilepsy as their primary medical condition. “The other seven percent reported epilepsy secondary to cancer, autoimmune conditions, neuropsychiatric conditions, chronic pain, insomnia/sleep disorders, or other conditions.” 

How They Did It 

The study participants employed a variety of cannabis-based products in the treatment of their epilepsy, including inflammation-reducing CBD, psychoactive tetrahydrocannabinol (THC), and several other cannabinoids that spanned anti-inflammatory cannabigerol (CBG), relaxant and sedative cannabinol (CBN), anti-nausea agent cannabidiolic acid (CBDA; the acidic precursor to CBD), and tetrahydrocannabivarin (THCV; the varin version of THC), which is known to reduce appetite. 

“For purpose of analysis, it is assumed that these participants were using an artisanal CBD product. A subset of artisanal CBD users reported also using known THC-dominant products containing high concentrations of both CBD and THC or products in which the primary chemical constituent was a minor cannabinoid such as CBG, CBN, tetrahydrocannabinolic acid (THC-A), CBD-A, or THC-V.”

The study also found the safety profile of CBD to be acceptable for patients and consumers, particularly for those using it to treat epilepsy. “Among the 280 baseline artisanal CBD users, the majority did not report an adverse effect.” 

What They Found

For those who suffer epilepsy and are seeking relief from CBD, the results of this scientific investigation reveal potentially limited efficacy of this popular cannabinoid for seizure management specifically. “No group differences were observed in seizure control based on self-reported number of past month seizures,” concluded the study’s authors.

Elaborated the scientists: “Seizure control did not differ based on artisanal CBD product use in this study. This may be related to a number of factors, including those that could not be controlled in [an] observational setting.”

Significant CBD Benefits Identified

However, the researchers noted that participants enjoyed a range of significant benefits from CBD, including “generally higher quality of life, lower psychiatric symptom scores, and improved sleep.” The study also reported that “artisanal CBD users” displayed considerably “better epilepsy medication tolerability.”    

Concluded the study, “Compared with controls, artisanal CBD users had greater health satisfaction.” It also found that the CBD-using epilepsy patients who participated in the research displayed “lower anxiety and depression.”

Despite its efficacy for many of the symptoms that accompany epilepsy, including psychological disorders like anxiety, depression, and insomnia, this particular study did not find that the cannabinoid CBD lowered the incidence or severity of seizure activity as experienced by those with epilepsy. 

Based on the observational and participant self-report nature of the study, the scientists noted that their results may be influenced by the loss of control that is inherent in observation research of this type. For a more comprehensive understanding of the topic, readers are encouraged to enroll in the Higher Learning LV seminar Understanding Cannabis.

Thanks for reading. Remember to #LearnAndTeachOthers at http://HigherLearningLV.co 

WSLCB Issues Memo Emphasizing Prohibition of Conversion of CBD to Delta-9 THC; Purchase or Sale of hemp-derived Delta-9 THC

August 5, 2021

To:                Cannabis Industry Members

From:           Chandra Brady, Enforcement & Education Division Director

Subject:      Prohibited: conversion of CBD to delta-9 THC; purchase or sale of hemp-derived delta-9 THC


Enforcement Bulletin 21-02

As the cannabis industry continues to evolve and progress, questions of the legality for manufacturing THC from hemp-based CBD created a need to assess and analyze statutory provisions related to this process.

Interpretive Statement #IS-21-02, Allowable Practices for a Holder of a Marijuana Processor License, concluded that processors licensed under RCW 69.50.363 may not legally convert CBD into delta-9 THC, as the license privileges do not allow them to convert CBD into THC. As the production of delta-9 THC falls outside the license privileges of a processor licensed by the LCB, that activity may be considered a controlled substances act violation, and a misuse of the processors license. Additionally, licensed processors may not sell or purchase any THC product not legally produced by a licensed marijuana producer.[1]

What does this mean for licensees?

  • Processors are not allowed to convert CBD into delta-9 THC.
  • Processors are not allowed to buy or sell delta-9 THC products not legally produced.
  • Retailers should not knowingly purchase products from processors which contain delta-9 THC converted from CBD. Nor should retailers sell such products to consumers.

How will WSLCB Enforcement and Education staff approach this in the field?

The Enforcement and Education team will approach this from an education-first perspective so we can help licensees achieve compliance. Our team has several tools to use to help; communication, basic education, administrative holds, warnings, notices to correct. If we identify licensees who are knowingly and intentionally violating rules and law or licensees who do not demonstrate a desire to achieve compliance, we will take appropriate enforcement action. 

Are there any exceptions?

There are no exceptions.

If you have any questions, please contact your assigned compliance consultant or enforcement officer.


[1] The interpretive statement also noted that it did not infer any approval for Marijuana Producer license holders to manufacture “marijuana” with a THC concentration greater than 0.3 percent on a dry weight basis from CBD.

FDA Warns Companies Illegally Selling Over-the-Counter CBD Products For Pain Relief

Products Listing CBD as Inactive Ingredient Cited for Unapproved Drug and Misbranding Violations

DISTRICT OF COLUMBIA: The U.S. Food and Drug Administration has issued warning letters to two companies for selling products labeled as containing cannabidiol (CBD) in ways that violate the Federal Food, Drug, and Cosmetic Act (FD&C Act). Specifically, the warning letters address the illegal marketing of unapproved drugs labeled as containing CBD. The FDA has not approved any over-the-counter (OTC) drugs containing CBD, and none of these products meet the requirements to be legally marketed without an approved new drug application. The letters explain that, as CBD has known pharmacological effects on humans, with demonstrated risks, it cannot be legally marketed as an inactive ingredient in OTC drug products that are not reviewed and approved by the FDA. Additionally, the letters cite substandard manufacturing practices, including failure to comply with current good manufacturing practices.

“The FDA continues to alert the public to potential safety and efficacy concerns with unapproved CBD products sold online and in stores across the country,” said FDA Principal Deputy Commissioner Amy Abernethy, M.D., Ph.D. “It’s important that consumers understand that the FDA has only approved one drug containing CBD as an ingredient. These other, unapproved, CBD products may have dangerous health impacts and side effects. We remain focused on exploring potential pathways for CBD products to be lawfully marketed while also educating the public about these outstanding questions of CBD’s safety. Meanwhile, we will continue to monitor and take action, as needed, against companies that unlawfully market their products — prioritizing those that pose a risk to public health.”

The FDA issued warning letters to:

The products that are the subject of the warning letters issued today have not gone through the FDA drug approval process and are considered unapproved new drugs. There has been no FDA evaluation of whether these unapproved drug products are effective for the uses manufacturers claim, what an appropriate dose might be, how they could interact with FDA-approved drugs or other products or whether they have dangerous side effects or other safety concerns.

The FDA has previously sent warning letters to other companies illegally selling unapproved CBD products that claimed to prevent, diagnose, mitigate, treat or cure various diseases, in violation of the FD&C Act.

Under the FD&C Act, any product intended to diagnose, cure, mitigate, treat or prevent a disease, and any product (other than a food) that is intended to affect the structure or function of the body of humans, is a drug. OTC drugs must be approved by the FDA or meet the requirements for marketing without an approved new drug application under federal law, including drug products containing CBD, regardless of whether CBD is represented on the labeling as an active ingredient or an inactive ingredient.

The FDA has not approved any CBD-containing drug products other than one prescription drug for the treatment of seizures associated with tuberous sclerosis complex, Lennox-Gastaut syndrome and Dravet syndrome in human patients.

The FDA has requested written responses from these companies within 15 working days stating how they will address these violations or providing their reasoning and supporting information as to why they believe these products are not in violation of the law. Failure to adequately address the violations promptly may result in legal action, including product seizure and/or injunction.

The FDA, an agency within the U.S. Department of Health and Human Services, protects the public health by assuring the safety, effectiveness, and security of human and veterinary drugs, vaccines and other biological products for human use, and medical devices. The agency also is responsible for the safety and security of our nation’s food supply, cosmetics, dietary supplements, products that give off electronic radiation, and for regulating tobacco products.

How CBD Can Help with Skin Problems

Anyone who’s suffered throughout their life with uncooperative skin has probably looked at many solutions to their troubles. Once they’ve exhausted other more obvious solutions, they may then cast a jaded eye towards skin cream that includes CBD as a significant ingredient.

What they may not understand clearly is whether a cream containing CBD will be helpful to them or not. Therefore, this article is aimed at providing some clarity on this issue.

One Itch or Three?

While it’s natural for the skin to itch when it is healing, it’s not as common or comfortable when that’s not the root cause. In which case, you’re trying to not scratch the area, but the itching is driving you’re a bit nutty!

If you’ve already tried antihistamine tablets and it didn’t do anything for you, then perhaps a cream with CBD will be worth trying now?

How will CBD help in this situation? Good question. What it does is disable the signal that’s communicating from the brain to your skin to create the itchy sensation. As a result, it’s felt less or removed entirely.

Protect the Skin from Damage

When out and about in the spring and summer months, being exposed to sunlight is almost inevitable. UV rays can cause cellular damage to the skin that’s irreversible and will eventually catch up with you. This is why sunbathing is detrimental, no matter how attractive a tan is.

The use of CBD cream can assist in preventing free radicals from UV rays that cause damage to the skin. When there’s no sun cream to hand, this alternative is great.

Remedy for Skin Breakouts

Chronic skin problems including minor to major breakouts are a real bugbear. Even if you’re a woman and able to cover over them with makeup, it’s still far from perfect. It’s also possible that the makeup will cause further skin irritation that won’t help either.

CBD cream helps with skin issues because it can reduce the build-up of oils on or below the surface that cause blocked pores in the first place. For people who suffer from an excess of oil on the skin that frequently creates fresh skin dilemmas, the use of CBD creams can reduce the frequency and severity of skin problems.

Avoid Aging as Rapidly

Avoiding aging is important to all of us. While we cannot stop the passage of time, we can at least try to stop our skin from looking significantly older.

CBD contains many antioxidants that shield the skin from harm including environmental-related damage. UV rays and air pollution are prevented from prematurely aging the skin when the cream is applied. Dark areas, fine lines, and pronounced wrinkles may be delayed as a result.

While no treatment is a cure-all for the way that the environment, pollution, and UV rays can ravage the skin, CBD cream provides added defense against them. Along with an effective cleaning and cleansing regimen, it can prove effective in keeping the skin looking its best.

 

 

Truss CBD USA, A HEXO Corp & Molson Coors Joint Venture, Launches Veryvell Sparkling CBD Water In Colorado

CANADA:  Truss CBD USA, a joint venture between HEXO Corp and Molson Coors Beverage Company, today announced the U.S. launch of VeryvellTM, a new line of non-alcoholic, sparkling CBD beverages, exclusively available in Colorado.

VeryvellTM is a hemp-derived, adaptogenic, sparkling CBD water now available to Colorado-based consumers in three flavours: Focus (Grapefruit Tarragon), Mind & Body (Strawberry Hibiscus) and Unwind (Blueberry Lavender). VeryvellTM is Powered by HEXOTM, the recognized quality and innovation behind award-winning products.

“We are excited to launch VeryvellTM in Colorado through Truss CBD USA, in collaboration with our partner, Molson Coors. Our joint venture with Molson Coors Canada saw Truss Beverage Brands become the number one choice for consumers in Canada and we are expecting similarly great results in the US.” said HEXO CEO and co-founder Sebastien St-Louis. “We have near-term plans to invest additional capital in the USA to support Truss CBD USA and to further execute on our Powered by HEXOTM strategy with other potential CPG partners, outside of beverages, with whom we are currently in ongoing negotiations.”

VeryvellTM is produced and distributed within Colorado state lines following the state’s established regulatory framework for hemp-derived CBD in food and beverages and is exclusively distributed by Coors Distributing Company. Truss CBD USA is distinct from Truss Beverages, Molson Coors and HEXO’s joint venture in Canada that focuses on non-alcoholic, cannabis-infused beverages.

FDA Warns Companies Illegally Selling CBD Products

DISTRICT OF COLUMBIA:  The U.S. Food and Drug Administration issued five warning letters to companies for selling products containing cannabidiol (CBD) in ways that violate the Federal Food, Drug, and Cosmetic Act (FD&C Act). All five warning letters address the illegal marketing of unapproved CBD products claiming to treat medical conditions. The warning letters include CBD products that are especially concerning from a public health perspective due to the route of administration, including nasal, ophthalmic and inhalation. In addition, they address violations relating to the addition of CBD to food, and the impermissible marketing of CBD products as dietary supplements. Two of the letters also address CBD products illegally marketed for pets, including a product for use in the eye.

“The FDA’s first priority is to protect the health and safety of Americans. Many questions remain regarding the science, safety, effectiveness and quality of products containing CBD,” said FDA Principal Deputy Commissioner Amy Abernethy, M.D., Ph.D. “We remain focused on exploring potential pathways for CBD products to be lawfully marketed while also educating the public about these outstanding questions of CBD’s safety. Meanwhile, we will continue to monitor and take action, as needed, against companies that unlawfully market their products — prioritizing those that pose the greatest risk of harm to the public.”

The warning letters were issued to:

The FDA has previously sent warning letters to other companies illegally selling unapproved CBD products that claimed to prevent, diagnose, mitigate, treat or cure various diseases, in violation of the FD&C Act. In some cases, there were further violations because CBD was added to food, and some of the products were impermissibly marketed as “dietary supplements.”

The products that are the subject of the letters issued today have not gone through the FDA drug approval process and therefore are considered unapproved new drugs. It is not known whether they are effective for the uses claimed in labeling, what an appropriate dose might be, how they could interact with FDA-approved drugs or other products or whether they have dangerous side effects or other safety concerns. In addition, the manufacturing process of these unapproved CBD-containing drug products has not been subject to FDA review as part of the human or animal drug approval processes, so it is not known what the manufacturing conditions of, or contaminant levels in these products may be.

Under the FD&C Act, any product intended to diagnose, cure, mitigate, treat or prevent a disease, and any product (other than a food) that is intended to affect the structure or function of the body of humans or animals, is a drug. New human and animal drugs must be approved by the FDA or conform to a “monograph” for a particular drug category, as established by FDA’s Over-the-Counter (OTC) Drug Review, before they can be legally marketed as drugs. CBD was not an ingredient considered under the OTC Drug Review.

The FDA has not approved any CBD products other than one prescription drug for the treatment of seizures associated with tuberous sclerosis complex (TSC), Lennox-Gastaut syndrome (LGS) and Dravet syndrome (DS) in human patients. CBD has not been approved as a food additive and does not meet the statutory definition of a dietary supplement.

The FDA has requested responses from the companies within 15 working days stating how they will address these issues, or providing their reasoning and supporting information as to why they think the products are not in violation of the law. Failure to adequately address the violations promptly may result in legal action, including product seizure and/or injunction.

The FDA, an agency within the U.S. Department of Health and Human Services, protects the public health by assuring the safety, effectiveness, and security of human and veterinary drugs, vaccines and other biological products for human use, and medical devices. The agency also is responsible for the safety and security of our nation’s food supply, cosmetics, dietary supplements, products that give off electronic radiation, and for regulating tobacco products.

FTC Announces Crackdown On Deceptively Marketed CBD Products

Companies made unsupported claims that their oils, balms, gummies, coffee, and other goods could treat serious diseases such as cancer and diabetes

DISTRICT OF COLUMBIA: The Federal Trade Commission today announced the first law enforcement crackdown on deceptive claims in the growing market for cannabidiol (CBD) products. The FTC is taking action against six sellers of CBD-containing products for allegedly making a wide range of scientifically unsupported claims about their ability to treat serious health conditions, including cancer, heart disease, hypertension, Alzheimer’s disease, and others.

The FTC is requiring each of the companies, and individuals behind them, to stop making such unsupported health claims immediately, and several will pay monetary judgments to the agency. The orders settling the FTC’s complaints also bar the respondents from similar deceptive advertising in the future, and require that they have scientific evidence to support any health claims they make for CBD and other products.

“The six settlements announced today send a clear message to the burgeoning CBD industry: Don’t make spurious health claims that are unsupported by medical science,” said Andrew Smith, Director of the FTC’s Bureau of Consumer Protection. “Otherwise, don’t be surprised if you hear from the FTC.”

The crackdown, Operation CBDeceit, is part of the Commission’s ongoing effort to protect consumers from false, deceptive, and misleading health claims made in advertisements on websites and through social media companies such as Twitter.

Each case the FTC is announcing today is described below:

Bionatrol Health, LLC

According to the FTC’s complaint against Utah-based companies Bionatrol Health, LLC and Isle Revive, LLC, and two former managers and owners, since at least December 2019 the respondents sold a CBD oil to consumers on two websites. Among other things, the respondents allegedly claimed without substantiation that their CBD product is safe for all users, treats pain better than prescription medications like OxyContin, and prevents and treats age-related cognitive decline and chronic pain. The respondents also claimed, without scientific evidence, that CBD oil is “medically proven” to improve a variety of conditions, according to the FTC’s complaint. In addition, the FTC alleges the respondents deceived consumers who ordered one bottle of their CBD oil by changing the order to five bottles without consumers’ consent.

The proposed administrative order settling the FTC’s charges prohibits the respondents from making certain prevention, treatment, or safety claims about dietary supplements, foods, and drugs without human clinical testing to substantiate the claims. It also requires competent and reliable scientific evidence for other health-related product claims, and prohibits the respondents from misrepresenting the cost of any good or service and from charging consumers without their express, informed consent. Finally, it requires the corporate respondents and individual respondent Marcello Torre to pay $20,000 to the FTC and to notify consumers of the Commission’s order.

Epichouse LLC (First Class Herbalist CBD)

According to the FTC’s complaint against Utah corporation Epichouse, LLC, which operated under several names, including First Class Herbalist, and the company’s founder and owner, John Le, since at least September 2019 the respondents sold several CBD products on their website, including oils, a pain-relief cream, coffee, and gummies.

Among other alleged unsupported claims, Epichouse and Le promoted CBD as safe for all users, able to treat pain better than prescription medications such as OxyContin, and able to prevent a wide range of serious conditions, including cancer, diabetes, and heart disease. In their advertising, they also falsely claimed that CBD is scientifically proven to improve many serious health conditions—including chronic pain and hypertension—and provide neurological benefit—such as preventing age-related cognitive decline—according to the FTC’s complaint.

The proposed administrative order settling the FTC’s charges prohibits the respondents from making certain prevention, treatment, or safety claims about dietary supplements, foods, and drugs, unless they have the human clinical testing to substantiate the claims. It requires them to have competent and reliable scientific evidence when making any other health-related product claims. Finally, the order requires the respondents to pay $30,000 to the FTC and notify consumers of the Commission’s order.

CBD Meds, Inc.

According to the FTC’s complaint against CBD Meds, Inc.; G2 Hemp, Inc.; and Lawrence Moses, a/k/a Lawrence D. Moses, Jr., individually and as an officer of the corporate entities, the two companies advertised CBD oil on their website and on YouTube. In their ads, the FTC contends, the Winchester, California-based firms made a number of false or unsubstantiated claims, including that CBD effectively treats, prevents, or mitigates serious diseases and conditions like artery blockage, cancer, glaucoma, autism, and schizophrenia, among many others. The respondents also falsely represented that some of the efficacy claims were scientifically proven or that the U.S. government has confirmed the health benefits of CBD.

The proposed administrative order settling the FTC’s charges prohibits the respondents from making certain prevention, treatment, or safety claims about dietary supplements, foods, and drugs, unless they have the human clinical testing to substantiate the claims. More broadly, it requires them to have competent and reliable scientific evidence when making any other health-related product claims. Finally, the order requires the respondents to notify consumers of the Commission’s order.

HempmeCBD

According to the FTC’s complaint against EasyButter, LLC, also d/b/a HempmeCBD, and its owner and officer Michael Solomon, since at least January 2018, the respondents have sold CBD products on their website, including CBD-infused shea butter, gummies, lozenges, honey sticks, vape pens, and oils. The complaint alleges that HempmeCBD claimed its CBD products could treat or cure serious ailments like cancer-related symptoms, substance abuse, and AIDS. The complaint alleges HempmeCBD lacked the scientific substantiation for such health claims and falsely claimed to have studies showing CBD is effective at treating autism.

The proposed administrative order settling the FTC’s charges prohibits the respondents from making certain prevention, treatment, or safety claims about dietary supplements, foods, and drugs, unless they have the human clinical testing to substantiate the claims. It also requires them to have competent and reliable scientific evidence when making any other health-related product claims. Finally, it requires the respondents to pay the FTC $36,254 and to notify consumers of the Commission’s order.

Reef Industries, Inc.

According to the FTC’s complaint against California-based Reef Industries, Inc.; Cannatera, Inc.; AndHemp, Ltd., and the companies’ three principals, the respondents have sold a variety of CBD products directly to consumers on their website and Twitter accounts since at least January 2019 and misrepresented the health benefits of CBD. The FTC alleges that the respondents made unsubstantiated claims that CBD can prevent, cure, mitigate, or treat diseases and serious health conditions, including Alzheimer’s disease, arthritis, autoimmune disease, and irritable bowel syndrome. The complaint also alleges the respondents falsely claimed that studies or scientific research prove that CBD is effective at treating, curing, or mitigating these diseases and conditions.

The proposed administrative order settling the FTC’s charges prohibits the respondents from making certain prevention, treatment, or safety claims about dietary supplements, foods, and drugs, unless they have the human clinical testing to substantiate the claims. More broadly, it requires them to have competent and reliable scientific evidence when making any other health-related product claims. Finally, it requires them to pay the FTC $85,000 and notify consumers of the Commission’s order.

Steves Distributing, LLC

According to the FTC’s complaint against Steves Distributing, LLC, d/b/a Steve’s Goods; and the company’s CEO Steven Taylor Schultheis, since beginning operations in 2018, the respondents have sold a variety of products containing both CBD and cannabigerol (CBG), which, like CBD, is a non-psychoactive compound derived from hemp. The company advertises its CBD and CBG products, including tinctures, gummies, capsules, topical balms, suppositories, bath balms, and coffee, on its website and through social media companies like Twitter.

The FTC alleges that the respondents claimed, without adequate substantiation, that their CBD and CBG products are effective alternatives to prescription medications and treat a wide range of diseases and serious health conditions, including Alzheimer’s disease, cancer, and diabetes. The complaint also alleges the respondents falsely claimed that their CBD and CBG products have antibacterial properties, prevent or reduce the risk of heart attacks, strokes, and other diseases, and that certain of these claims were supported by scientific evidence.

The proposed administrative order settling the FTC’s charges prohibits the respondents from making certain prevention, treatment, or safety claims about dietary supplements, foods, and drugs, unless they have the human clinical testing to substantiate the claims. More broadly, it requires them to have competent and reliable scientific evidence when making any other health-related product claims. Finally, it requires the respondents to pay the FTC $75,000 and notify consumers of the Commission’s order.

The Commission votes approving each of the six administrative complaints and proposed consent orders were 5-0, with Commissioner Rohit Chopra and Commissioner Christine S. Wilson issuing separate, concurring statements. A complete list of respondents can be found in the complaint for each respective case.

The FTC will publish a description of the consent agreement package in the Federal Register soon. The agreement will be subject to public comment for 30 days after publication in the Federal Register after which the Commission will decide whether to make the proposed consent order final. Instructions for filing comments will appear in the published notice. Once processed, comments will be posted on Regulations.gov.

NOTE: The Commission issues an administrative complaint when it has “reason to believe” that the law has been or is being violated, and it appears to the Commission that a proceeding is in the public interest. When the Commission issues a consent order on a final basis, it carries the force of law with respect to future actions. Each violation of such an order may result in a civil penalty of up to $43,280.

Canopy Growth Expands Beverage Portfolio with Launch of First CBD-Infused Beverage Line Quatreau

New Product Line Features A Range of Naturally Flavoured Cannabis-Infused Sparkling Waters In Both CBD-only and Balanced (CBD + THC) Offerings

CANADA: Canopy Growth, a world-leading diversified cannabis, hemp, and cannabis device company, today announced the launch of Quatreau, a new line of premium CBD-infused beverages. The naturally flavoured sparkling waters are Canopy Growth’s first CBD-infused drinks, with both CBD-only and “balanced” (CBD + THC) offerings available in Canada. Launched on the heels of incredible growth in sales from the Company’s THC-infused beverages, released earlier this year, Canopy Growth is uniquely positioned to win market share in the CBD beverage space.

“We are proud to debut our first CBD-infused beverage brand in Canada, where we already lead the cannabis-infused beverage category, at a price point that delivers both quality and value to consumers,” said David Klein, CEO, Canopy Growth.  “We created Quatreau as an alternative to sugary, caffeinated beverages or even alcohol. With both CBD-only and “balanced” (CBD + THC) offerings in four natural  flavours, Quatreau meets the needs of discerning cannabis consumers.”

Canopy Growth plans to continue developing category leading brands that are driven by consumer insights, product-focused, with industry leading scientific formulation. Building on the successful launch and strong sales of THC-infused cannabis beverage brands Tweed, Houseplant and Deep Space, Canopy is poised to continue leading the cannabis space with the launch of Quatreau CBD-infused sparkling water, a consistent CBD product in a beverage format that is familiar to consumers.

Quatreau’s naturally flavoured Canadian product line includes four offerings named:

  • Quatreau Cucumber + Mint (contains 20 mg of CBD and < 1 mg of THC)
  • Quatreau Passion Fruit + Guava (contains 20 mg of CBD and < 1 mg of THC)
  • Quatreau Ginger + Lime (contains 2 mg of CBD and 2 mg of THC)
  • Quatreau Blueberry + Açai (contains 2 mg of CBD and 2 mg of THC)

For more information, visit quatreauwater.com