Thursday, August 21, 2025
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Feds Go After Golden Sunrise Nutraceuticals for Fake Covid19 Cure

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The Federal Trade Commission (FTC) sued Golden Sunrise Nutraceutical for allegedly deceptively advertising its $23,000 COVID-19 treatment plan as “FDA accepted.”

Golden Sunrise Nutraceutical is a company based in Porterville, California. The company sells a variety of dietary supplements and claims that these products provide numerous health benefits including curing serious diseases.

The federal consumer protection watchdog also names Golden Sunrise Nutraceutical’s CEO Huu Tieu and Medical Director Stephen Meis as defendants in the case.

In the lawsuit, the FTC noted that the defendants are marketing their dietary supplements through four plans of care: 1) Primary Plan of Care; 2) Emergency D-Virus of Care; 3) Metabolic Plan of Care, 4) Cancer Plan of Care. They claimed that these treatment plans provide consumers with safe and effective treatment for serious diseases.

In March 2020, Golden Sunrise Nutraceutical started marketing its Emergency D-Virus plan as a treatment for COVID-19.

The FTC alleged that the defendants falsely claimed in its advertisements on billboards, websites, and social media that its herbal supplements ImunStem, Aktiffvate, and AnterFeerons are “uniquely qualified to treat and modify the course of the Coronavirus epidemic in CHINA and other countries.”

Additionally, the FTC alleged that the defendants falsely claimed that people who are frequently using one of the supplements included in the Emergency D-Virus treatment plan can expect “disappearance of viral symptoms within two to four days.”

Furthermore, the FTC alleged that the defendants are deceptively marketing their products as treatments for cancer, Parkinson’s disease, and many other serious illnesses.

In reality, the treatments are comprised mainly of different herbs and spices and the defendants’ health claims are unproven. Some of Golden Sunrise Nutraceutical’s treatment plans cost as much as $170,000 to $200,000, according to the Commission.

Moreover, the FTC alleged that the defendants falsely claimed that the Food and Drug Administration (FDA) reviewed and accepted its products and treatment plans.

In April 2020, the FTC sent a warning letter instructing the company to immediately remove all its false and misleading advertisements that its products can prevent, treat, or cure COVID-19. Despite the warning, the defendants continued deceptively advertising the Emergency D-Virus treatment plan as a “New Covid-19 Treatment.”

In a statement, FTC Bureau of Consumer Protection Director Andrew Smith said, “We warned the defendants not to falsely market their product as an effective treatment for COVID-19, but they didn’t stop. As this case makes clear, the FTC is prepared to sue companies that continue to make deceptive health claims about COVID-19 or other serious diseases.”

Why Evergreen Messages Fail During Covid19

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Mobile Email Performs Better

If advisors want to reach clients, they should make it timely and personnal, according to Snappy Kraken CEO Robert Sofia.

During the market volatility that emerged as the coronavirus spread across the world, consumer engagement with timely content skyrocketed, said Sofia when reporting the results of Snapppy Kraken’s “How 2020 Has Changed Financial Adviser Marketing” report last week.

After Snappy Kraken pulled data from the first six months of 2020, when it deployed 150,000 social media post, over 12,500 digital marketing campaigns and sent 5 million emails on behalf of advisros, Sofia was able to distill five key lessons, which he will share with attendees during his “Updated 2020 Half-Time Review: The Latest Financial Adviser Marketing Trends Revealed In New Study” webcast hosted by Financial Advisor  magazine on Wednesday, August 12 at 2 p.m. ET.

“The biggest shift we saw was in the fundamental performance of two types of content,” he said. Engagement with evergreen content, which includes general content about things like Roth conversions, 401(k)s and investment selection, dropped by 42%.

Simultaneously, the engagement with timely content, which is content relevant to current events in the world or in clients’ lives, rose by 370%.

“Here’s the point,” said Sofia. “If you are reliant on your normal marketing strategy, the things you do 24-7-365 in a normal time, if you do those things during a time of crisis, it won’t matter. When there’s a crisis, everybody’s mind then shifts to that crisis, and how it affects that person, and that applies to the financial services you provide.”

To optimize their results, advisors may have to change ther marketing on a monthly or weekly basis to keep up with changing trends, said Sofia.

FTC Starts Scammer Search Engine

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The FTC Building

The Federal Trade Commission (FTC) has created a search tool for researching information about identity theft and other fraud issues specific to your state.

EXPLORE DATA is the FTC’s Consumer Sentinel Network data about consumer protection topics based on millions of reports from people across the country. You will be able to research the top complaints, track the latest trends, and download charts for presentations or reports. You can also find out about refunds to consumers from FTC law enforcement cases, where the money went, and how much people got back.

For instance, according to the FTC data, since 2018, 96,960 Massachusetts consumers have received over $17-million in refunds as part of FTC consumer protection actions.

From January through June 2020, Massachusetts residents have filed 29,103 complaints to the National Do Not Call Registry, over 20,000 were robocalls on topics ranging from debt reduction to home improvement, and computer tech support and lotteries or sweepstakes.

To stay up to date on scams that could affect you and your community, you can sign up for the FTC’s free Consumer Alerts emails. You can report consumer complaints at ftc.gov/complaint.

Lead Generation Platform Developer TCPA Liability Considerations

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As previously blogged about here, software developers that are engaged to design lead generation management platforms for third-party use in conjunction with direct marketing campaigns, specifically, telemarketing, should be aware of a number of factors related to potential liability for the actions or inactions of their clients.

Consider that platform providers can potentially be held liable for Telephone Consumer Protection Act violations committed by platform users where the former “knowingly” allows clients to use the technology for unlawful purposes.  Importantly, in a 2015 order, the Federal Communications Commission stated that initiating a telephone call can apply to either the person or entity that takes the steps necessary to physically place a telephone call or the person or entity that is “so involved in the placing of a specific telephone call as to be deemed to have initiated it.”

The absence of actual knowledge, however, may not necessarily be a defense for platform developers.  For example, consider what a developer “should” reasonably know, and how active a role a developer plays in the creation, control, initiation and/or dissemination of promotional content (e.g., telephone calls).  Responsibility for the specifications, requirements and/or deliverables of the software may also be deemed relevant by a court when assessing whether platform provider liability is triggered.

Whether a platform developer can be held liable for providing the software used for direct marketing purposes is not always a black and white analysis.  Certainly, the totality of the specific facts and circumstances, including, the right to control and role in the underlying transmission, are relevant when assessing the identity of the “caller,” and legal responsibility for ensuring TCPA and Telemarketing Sales Rule compliance.

Applying the factors in the 2015 FCC order, the FCC and FTC have found dialing platform providers directly liable for violations of the TCPA and TSR. 

Recently, the FTC ordered a dialing platform provider to pay $75,000 and review all pre-recorded calls and to terminate relationships with clients that were using the dialing platform to make illegal calls. The court determined that the platform provider provided “substantial assistance” to clients that were using the technology to initiate unlawful telephone calls and that it r consciously avoided knowing that the platform was being used in an unlawful manner. 

In another recent decision, the FCC fined a dialing platform provider approximately $2.8M for permitting telemarketers to utilize its software to make robocalls to mobile phones without lawfully required consent.  This decision is particularly noteworthy because the fact that customers were required to agree to terms that included an obligation to comply with applicable legal regulations was not deemed exculpatory.

The 2015 FCC ruling makes clear that “a provider of auto-dialing services cannot blithely sit back and blame his customers for any TCPA violations that result from their use of his service.”

It is not difficult to imagine regulatory agencies and plaintiffs’ attorneys pursuing similar third-party accountability remedial approaches in the context of other forms of direct marketing.  Providers that simply assume they are passive conduits and immune from liability under the TCPA, the TSR or other applicable legal regulations when negotiating contracts, engaging in the development process and maintaining involvement in promotional campaigns may unknowingly be exposing themselves to extraordinary liability. 

Consult with experienced FTC defense lawyer to discuss liability mitigating steps designed to ensure platform users are not operating in a non-compliant manner, including, but not limited to, utilizing responsible and professionally drafted contracts; designing and implementing reasonable customer screening, vetting and due diligence protocols; implementing an appropriate certification process; and ensuring that appropriate remedial action is taken in the event unlawful conduct is known or reasonably should be known.

Richard B. Newman is an advertising and marketing practices attorney at Hinch Newman LLP. You can follow him on Twitter @FTC Defense Lawyer.

Informational purposes only. Not legal advice. May be considered advertising material.

Every CPG Brand will be a Direct Response Brand Going Forward

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Sometimes it takes a crisis to challenge conventional wisdom. Not long ago, an imaginary line separated brand marketing, with its focus on awareness and devotion to subjective “big ideas,” from direct response and its laser-focus on measurable outcomes like driving sales. Many firms either practiced one or the other, but not both. Or, if they did run both brand and direct response operations, they typically did so inside siloed marketing organizations. Today, the story is changing.

Across industries, DTC disruptors like Peloton, Casper Mattress, and Warby Parker have seized market share. Large CPG holding companies like Unilever and P&G have responded by acquiring DTC firms like Dollar Shave Club and Billie, respectively. But DTC acquisitions were only the start. Increasingly, even traditional CPG brands are turning to direct response, due to a confluence of trends that includes a greater emphasis on first-party data, better media attribution tactics, and the need to tie marketing to business outcomes. But above all, traditional CPG brands must embrace direct response because doing so brings them closer to their customers.

CPG brands can go direct, but they need to proceed with common sense

A few years ago, Coca-Cola ran a direct response experiment with its “Share a Coke” campaign. The idea was a good one—create a more personal relationship with consumers and inspire shared moments of happiness. But the payoff (your name on a Coke) was more gimmick than game plan. That is, Coca-Cola gave consumers a wow-factor, but none of the marketing, sales, or distribution infrastructure the company created to pull off the stunt brought them closer to becoming a direct marketing brand.

Of course, the soda wars are nothing if not symmetrical. Recently, Pepsi did direct response too, but instead of personalizing the product, the brand personalized the sale via DTC websites. Yes, Pepsi products are still largely bought through retailers and at venues and restaurants, but in the midst of a pandemic, Pepsi has also created viable marketing, sales, and distribution infrastructure that serves as a direct conduit from brand to consumer.

This trend is playing out broadly across CPG brands. For the most part, however, brands have turned to various platforms such as Instacart, Pinterest, and Instagram in order to pull off a DTC pivot. But shifting online and minimizing the number of middlemen between brand and customers isn’t exactly the same thing as “owning” the customer relationship. In the short-run, this strategy might be a good hedge against consolidated power in the e-commerce space, but as CPG brands push toward a closer relationship with consumers, they must remember the lesson of Amazon—those that fulfill the customer’s order, know the customer better than they know themselves.

 It’s about sales, but it’s really about relevance

Brands with first-party data are the haves of marketing, and those without are the have-nots. But instead of building the customer relationships that yield data, many have-nots,  including CPG brands, continue to rely on third-party data to improve media targeting and drive revenue.

That’s one reason why PayPal spent $4 billion to acquire a shopping coupon plug-in called Honey. As Business Insider put it, “[the] business model where businesses are paid for driving transactions is unequivocally the model of the future.” Brands that outsource the key aspects of that model do so at their long-term peril because they ignore a fundamental law of business: know your customer.

Direct response brands are many things to many people, but their common denominator is that they know their customers better than anyone else. To achieve that knowledge, direct response brands have to be incredibly sales-driven. But sales-driven isn’t a shorthand for tunnel vision or a bottom-line mentality, despite what some brand marketers may think. In fact, sales is a meme that describes relevance.

In good times, that hyper-focus on relevance informs every decision, from product, to marketing, to distribution. Direct response brands miss the mark sometimes, but they miss small and adjust quickly because their DNA is coded to seek out relevance. And it’s that hyper-focus on relevance that pays dividends when a massive disruption like a pandemic creates widespread uncertainty. Consider the early, chaotic months of the pandemic. Brand marketing was largely criticized for either going dark or pushing out tone deaf messages. In contrast, most direct response brands didn’t go dark or appear tone deaf, because they knew precisely where to meet consumers, even at a moment when consumer behavior was changing by the hour.

 There is no going back

For all the talk of “getting back to normal,” there’s no reason CPG brands should reverse course on the progress they’ve made on the direct marketing front. Why would the brand give up the data-rich consumer relationship? Why would the business forgo the flexibility and resiliency of an alternative conduit to the consumer? And why would the consumer forgo the convenience and savings of going direct?

The answers should be obvious—there is no going back. But that doesn’t mean marketers have done a mental reset yet, nor have marketing organizations had the time restructure themselves. Nevertheless, CPG brands have glimpsed the future in this moment. They should build on whatever DTC initiatives they’ve run by embracing direct response as their marketing engine, not a sideshow. Because those CPG firms that use direct response to drive operations are also the same brands that can truly say they know their customers better than anyone else.

Button Announces Partnership with Awin Affiliate Network

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 Button, a mobile commerce technology company, today announced the launch of Reach™, the company’s newest product that offers its deep linking and app-tracking technology as a service to affiliate network traffic. Awin, a relatively new affiliate network that claims 205,000 contributing publishers and 14,600 brands, is the first network to integrate with Button through Reach™ to unlock app installs and drive incremental growth for their brand partners.

Affiliate marketing spend is rapidly growing and is due to surpass $8 billion by 2022, according to Statista. Through the pandemic, affiliate budgets could prove resilient as brands are increasingly focused on the strong return on investment and guaranteed sales the channel offers, according to Awin.

With the launch of Reach™ and the continuation of the partnership between Button and Awin, Awin’s brand partners now have their mobile traffic optimized through the higher-converting app channel. Reach™ enables brands to capture higher-value users through installs and improve the accuracy of affiliate tracking in their app, publishers to benefit from higher payouts through purchases made by app shoppers, Awin to track app installs and sales for its partners, and consumers to get a more seamless shopping journey on mobile.

Early Reach™ tests revealed that a major brand on Awin’s affiliate network was able to outperform standard mobile web affiliate traffic by 50%. Furthermore, it was proven that 10% of shoppers who made a purchase had installed that brand’s app and that 60% of shoppers who installed that brand’s app made a purchase within 30 days. As a result of Reach™, Awin is able to unlock app installs and sales, enhance the mobile shopping experience for their partners, and get accurate app tracking—driving incremental growth by tapping into the full potential of mobile affiliate traffic.

“Awin strives to be at the forefront of performance marketing, both through our own innovation and working with cutting-edge partners. We’re excited to further drive forward the channel by partnering with Button to provide more value to our brand partners in-app,” said Paul Stewart, Global Head of Strategic Partnerships and Innovation at Awin, “With Reach™ enabling Awin to be a first mover in the affiliate app space, we look forward to sustaining our growth as a global network trusted by our partners to deliver unparalleled performance.”

“The only reliable channels of app acquisition for retailers are Facebook and Google. We hear from all our biggest retail partners that affiliate marketing represents 15% of their marketing spend, and is also the most profitable channel for them. Yet, it has historically accounted for zero app installs,” said Michael Jaconi, Co-Founder and CEO of Button. “Through Button’s partnership with Awin via Reach™, we are unlocking the true potential of the affiliate channel for app acquisition.”

The Upcoming Bust of the Hand Sanitizer Market

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The FDA is expanding their warning about certain hand sanitizers made in Mexico due to the potentially toxic ingredient methanol.

Hoping to clean up in the hand sanitizer business, a horde of entrepreneurs have upended the category by attempting to capitalize on an opportunity driven by the COVID19 virus.  In a buying frenzy, product flew off of store shelves creating massive demand.  A simple formula and a ready supply of ingredients has allowed many small businesses to manufacture product for sale and distribution to consumers.   As traditional manufacturers attempt to increase inventories including an increasing number of ad hoc opportunists, oversupply seems highly likely.

Considering the sheer number of online offers for product one might expect a glut on the market.  On Amazon alone, we found 310 listings for “hand sanitizer” selling from $11,543 for a 265 gallon container ($2.94/oz.) to $7.00 for a bottle with a single ounce.  By contrast, Dollar General Stores sells a 2 ounce bottle of hand sanitizer for as little as $1.00.  These wide variations in pricing create much confusion for the public as they attempt to secure a continuing supply of the product.  However, the demand appears undiminished.

The government estimates that the hand sanitizer market will grow to $5.1BB by 2024, a 600% increase.  The product’s growing demand brings some big players into a once fragmented market. Exxon/Mobil announced the production of 160,000 gallons of hand sanitizer in their Louisiana refinery with a plan to donate to local and national health care providers and first responders.  And, they are not alone in this endeavor.  Many major distillers including Anheuser Busch and Bacardi are currently manufacturing hand sanitizer to donate to facilities in their local communities.

Major retail discounters like The 99¢ Store, Dollar General and others including Walmart and Target currently sell hand sanitizer at low prices.  Even though the demand is through the roof, retailers and discount store prices are stable with no indication of substantial increases.  It raises the question, with so many producers of hand sanitizer, will the market become oversaturated?

The supply chain indicates a growing demand for hand sanitizer but there are other issues like the shortage of plastic containers and their perceived effect on the environment.  FDA requires that the only pharmaceutical grade ingredients are used in the manufacture of sanitizer and these components are in short supply.  Many manufacturers indicate that they have a reduced capacity because of supply chain interruptions.  The fear is that the market will be unable to meet the growing demand.  However, this fear has not materialized.

In the Consumer Packaged Goods category, the number of SKUs should diminish as the pipeline is filled by traditional manufacturers.  The 300 plus sellers on Amazon will face a dilemma when the demand for high-priced product disappears.  Among this group and others attempting to cash-in on COVID19, fear they may have priced themselves out of the market.  They face the choice of reducing their pricing to competitive levels or absorb a large amount of unsold inventory.  One might expect that with so many producers, an eventual oversupply may develop.  However, we can expect COVID19 to become a continuing reality that may well extend into the distant future.  The supply chain takes time to fill the pipeline but we can expect this product to be around for a long, long time.

FTC Sues Kevin Lipsitz of SuperGoodDeals.com for PPE Scam.

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The Federal Trade Commission (FTC) filed a lawsuit against an online marketer for allegedly falsely promising consumers next-day shipping of face masks and other personal protective equipment (PPE) necessary to prevent the spread of the novel coronavirus (COVID-19).

In the lawsuit, the FTC noted that SuperGoodDeals.com, Inc, and its owner, Kevin Lipsitz, tried to take advantage of increasing consumers demand for PPE due to the COVID-19 pandemic that has already claimed the lives of 132,056 people in the U.S. as of July 9.

The defendants started selling facemasks and other PPE through their website in March 2020. They claimed that the PPE was in stock and ready to ship the next day.

Allegations against SuperGoodDeals and its owner

The defendants stated, “We pride ourselves on fast order processing. Pay Today, Ships Tomorrow!” on the shipping and delivery page of their website. They also promised to respond to consumer inquiries “within 1 business day or less.”

The FTC alleged that the defendants’ promises were false in many cases. In fact, it took weeks for the defendants to ship orders, they failed to inform consumers of the delay, and ignored repeated demands for refunds.

Additionally, the Commission alleged that SuperGoodDeals and Lipsitz were selling counterfeit products through their website.

The defendants violated Section 5(a) of the FTC Act,15 U.S.C. § 45(a), which prohibits unfair or deceptive business practices. They also violated the Mail, Internet, or Telephone Order Merchandise Rule (MITOR), according to the Commission.

In a statement, FTC Consumer Protection Bureau Director Andrew Smith said, “Unscrupulous merchants are taking advantage of consumers in their hour of need by not delivering goods—including masks and other personal protective equipment—as promised, and failing to provide required refunds. The FTC will not tolerate this, and we are working closely with criminal authorities to put a stop to it.”

Separately, the U.S. Attorney’s Office for the Eastern District of New York filed a criminal complaint against Lipsitz for allegedly violating the Defense Production Act and defrauding consumers.

U.S. Attorney Richard Donoghue said, “The defendant allegedly took advantage of the pandemic and the public’s urgent need for life-saving PPE to enrich himself illegally. Our Office and the Department’s COVID-19 Hoarding and Price Gouging Task Force will continue working tirelessly to put an end to such conduct.”

Price gouging and other fraudulent activity in response to the COVID-19 pandemic has been seen all over the U.S. The FTC and state authorities have been doing their best to combat retailers who seek to take advantage of peoples’ fear.

FTC Stops Thrive & Whole Leaf Organics Covid19 Scam (Again!)

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The California-based marketer of a supplement called Thrive, which consists mainly of Vitamin C and herbal extracts, is barred from continuing to make baseless claims that it can treat, prevent, or reduce the risk of COVID-19, under an administrative settlement with the Federal Trade Commission.

The FTC proposed order also bars the marketer of Thrive, Marc Ching, from making similarly unsupported cancer treatment or prevention claims for products containing CBD. The case against Ching is the FTC’s first against a marketer of a supposed COVID-19-related health product. In April 2020, the FTC announced that Ching agreed to a preliminary federal court order that imposed similar terms.

“There’s no proof that this product will prevent or treat COVID-19, and no proof that any CBD product will treat cancer,” said Andrew Smith, Director of the FTC’s Bureau of Consumer Protection. “This case, and the hundreds of warning letters we’ve sent, demonstrate that we will remain vigilant against companies that lack the scientific proof to back up their claims.”

According to the FTC’s administrative complaint, since at least December 2018, Ching has advertised and sold Thrive online, through his Whole Leaf Organics website, and in March 2020 he began marketing it as an “anti viral wellness booster” that treats, prevents, or reduces the risk of COVID-19. In addition, the FTC alleged Ching falsely stated that these benefits of Thrive were clinically proven.

The complaint also alleged that Ching used his Whole Leaf Organics website to advertise and sell three CBD-containing products, CBD-EX, CBD-RX, and CBD-Max, falsely claiming they were effective cancer treatments. CBD-EX is an ingestible capsule consisting mainly of a combination of cannabidiol and herbal extracts. CBD-RX and CBD-Max are oils composed primarily of CBD and hemp extract.

The FTC, CBD and the Law During Covid19

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Amid the COVID-19 pandemic, a number of cannabis companies that advertised CBD products as effective in preventing or treating COVID-19 without obtaining U.S. Food and Drug Administration (FDA) approval have become targets of Federal Trade Commission (FTC) enforcement actions. By way of example, on April 22, 2020, the FTC filed an administrative complaint against Marc Ching, individually and as Whole Leaf Organics, to cease unfair or deceptive practices and false advertisements for products affecting commerce in violation of the Federal Trade Commission Act. Two days later, the FTC petitioned the Unites States District Court, Central District of California, to enter a temporary restraining order and grant a preliminary injunction enjoining Marc Ching and Whole Leaf Organics from disseminating false or unsubstantiated advertisement claims that the CBD products marketed as CBD-EX, CBD-RX, and CBD-Max treat cancer, and the CBD product marketed as “Thrive” prevents or reduces risk associated with COVID-19. In response to the FTC complaint, Marc Ching and Whole Leaf Organics agreed to a preliminary order to cease advertising these claims.

The fact that the FTC filed this lawsuit presents a notable departure from its previous enforcement activity and that of the FDA. This suit demonstrates the FTC’s commitment to protecting Americans from harm caused by products falsely claiming to prevent or treat serious diseases, such as COVID-19. In fact, on April 20, 2020, the FTC commented that “[a]t a time when Americans are looking for any hope and solutions to the COVID-19 pandemic, we’re increasingly concerned about the deceptive practices some marketers can, have, and will employ.”

Before the pandemic, in late November, the FDA began sending warning letters to companies who marketed CBD products in interstate commerce based upon alleged violations of the Federal Food, Drug, and Cosmetic Act (FD&C Act). In particular, CBD companies that received these warning letters were accused of using product webpages, online stores and social media as channels to advertise CBD product claims associated with preventing, diagnosing, mitigating, treating and/or curing serious diseases, such as cancer, or for other unsubstantiated uses, such as therapeutic uses for humans and/or animals. Other violations cited marketing CBD products as dietary supplements and adding CBD to human and animal foods. Under the FD&C Act, any product intended to treat a disease or otherwise have a therapeutic or medical use, and any product (other than food) that is intended to affect the structure or function of the body of humans or animals, is categorized as a drug, which must be approved by the FDA. Therefore, if a CBD product is marketed in such a way, the manufacturer is required to first obtain approval from the FDA.

Prior to the enforcement action filed in April, the FDA had issued a warning letter to Whole Leaf Organics concerning advertising CBD-EX, CBD-RX, and CBD-Max products as “effective when combating cancer cells …. It has been able to kill cancer cells, as well as prevent additional cells from growing.” The unapproved new drugs were being sold in violation of section 505(a) and 301(d) of the FD&C Act. The FDA warning provided Whole Leaf Organics with 15 days from the date of receipt of the letter to take corrective action. However, it appears that Whole Leaf Organics did not cease making such claims until after the enforcement action was filed.

On April 6, 2020, the FDA issued similar warnings to other CBD manufacturers who claimed that their CBD products were safe and/or effective for the treatment or prevention of COVID-19. For instance, Native Roots Hemp claimed that cannabis “speeds recovery” from COVID-19, and touted cannabis resin as an “antiviral” that “inhibits cell proliferation.” Indigo Naturals suggested that CBD boosts T-cells with “powerful weapons” that could ward off COVID-19. The warning letters sent by the FTC to both Native Roots Hemp and Indigo Naturals alleged that the products being sold were unapproved new drugs and therefore violated sections 505(a), 301(a) and (d) of the FD&C Act. The FDA demanded that each company take immediate corrective action, including removing all misleading representations that their products are safe and effective for COVID-19.

Upon receipt of an FDA warning letter, a company typically has 15 days to respond. However, due to the emergent nature of the COVID-19 pandemic, Native Roots Hemp and Indigo Naturals were given just 48 hours to comply. Pursuant to applicable regulations, failure to respond to an FDA warning letter may result in legal action without further notice, including, without limitation, seizure and injunction.

 

Given the FDA’s ramped-up enforcement efforts, it is anticipated that we will see additional warning letters, lawsuits, and injunctive action taken in the foreseeable future in order to protect consumers during the pandemic. The FDA’s position has been clearly articulated when it stated, “Let’s be clear: companies making these claims can look forward to an FTC lawsuit like this one.”

 

 

FTC Settles Another Health Claim Action

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“Treats Chronic Pain… Clinically Proven… Smart Device… Approved by the FDA…” These are all claims the Federal Trade Commission (FTC) says defendants made advertising the Willow Curve, a low-level light therapy device  (LLLT), and all of which the FTC says are false and deceptive. In a settlement announced June 25, 2020, the Willow Curve LLLT device defendants will be subject to a $22 million judgment which includes penalties being paid by two individual physicians who led the involved company LLCs. Defendants also will be prohibited from future allegedly deceptive refund and native advertising campaigns.

“’When LLLT sellers say their devices will relieve pain, they’d better have the scientific proof to back it up,” said Andrew Smith, Director of the FTC’s Bureau of Consumer Protection, in a June 25 press release. ‘People looking for drug-free pain relief deserve truthful information about these products.’”

FTC Complaint Causes of Action. The complaint asserts  the following six counts against defendants which target all aspects of the allegedly improper marketing and sales of the product.

  1. False or Unsubstantiated Efficacy Claims
  2. False Proof Claims
  3. False Claims About FDA’s Review
  4. Deceptively Formatter Advertisements
  5. Defendants’ Provision of Means and Instrumentalities of Deception
  6. False Refund and Risk-Free Claims

The complaint also contains substantial snapshots of advertising and marketing materials, including scripting of infomercials, native content “research” materials, and alleged testimonials.

All of the claims are based on alleged violations of the Federal Trade Commission (FTC) act, specifically  Sections 5(a) and 12, 15 U.S.C. §§ 45(a) and 52, which prohibit deception in connection with the manufacturing, labeling, advertising, marketing, distribution, and sale of products. Relief is sought under Section 13(b), 15 U.S.C. § 53(b), which permits the FTC to obtain permanent injunctive relief, rescission or reformation of contracts, restitution, the refund of monies paid, disgorgement of ill-gotten monies, and other equitable relief for defendants’ acts or practices in violation of the FTC Act.

Scientific Proof for Health Claims. This is the first FTC enforcement settlement involving an LLLT.

The LLLT “is an FDA registered, software controlled, handheld device for joint pain relief. It combines the documented benefits of safe laser, infrared, and LEDs in one device that produces safe medical grade pain relief at a fraction of the cost.”

Among other statements, certain of the Willow Curve advertisements claim: “When applied, the Curve’s diagnostic sensors gather information from your skin. Then the smart device adjusts the photonic and thermal kinetic energies, stimulating the body’s natural pain-relieving and anti-inflammatory responses. It’s not science fiction. It’s a trusted, effective breakthrough in pain relief technology.”

The product marketing also touted “dynamic multi-band alternating pulse therapy (ATP) the body tissues absorb to

  • Enhance central pain management systems function,
  • Spark the body’s opioid receptor,
  • Reduce inflammatory pain response and accelerate tissue healing
  • Suppress sensory fatigue (adaptation), improving extended pain relief momentum and recovery…”

According to the FTC, none of this was borne out by scientific proof specific to the Willow Curve device. The FTC alleges no clinical studies prove any of the numerous health treatment and benefit claims asserted by Defendants’ advertising. The FTC contends Defendants’ representation that the product’s treatment benefits are equal to that of prescribed drugs or surgery. The FTC alleges that the FDA has not approved the product or corroborated any of the purported health claims defendants have made.

Purported “Independent Journalism”. Count IV challenges the formatting and appearance of certain content which appear on the webpage to be independent journalism stories about the product, but which actually were drafted by the marketing team.  Moreover, the content is formatted to appear similar to other independent content on the same pages. It is not differentiated or identified as advertisement.  The FTC contends that such formatting is likely to cause consumer confusion and may mislead consumers.

Refunds Delays & Charges. The complaint also alleged that defendants did not comply with their representations regarding a “risk free money back” guarantee. The FTC alleges instead that “consumers who returned the device had to pay shipping and handling costs and often did not receive a refund at all or had to wait more than a year for it.” One initial flag for the FTC is that returns volumes were high, as high as one-third of purchases at a certain point in time.

Consumer Class Action & Regulatory Litigation Risk for Your Products. Whether you are the maker or retailer or influencer/spoke person, you may have risk if the marketing claims are not true. In addition to the risk from federal regulators like the FTC, state Attorneys General and consumers can assert claims for unfair and deceptive advertising and marketing practices under applicable state laws. Here, the retailers and distributers who leveraged the deceptive defendant supplied product marketing materials were not also named as targets. But in consumer civil litigation, they might have been. So too perhaps could have been influencers or spokespersons, whose reputations were used to establish consumer trust and drive product sales. While these additional targets may have a variety of defenses to assert, litigation claims are disruptive and expensive and can dilute brand and diminish reputation.  Product claims should be carefully vetted. Claims regarding specific efficacy and/or physical improvement ought to be well documented through scientific proof. When challenges arise, the nature and credibility of that proof will drive the outcome.

OfferGlobe and Steve Mandes Illegal Spammers and Scammers Review.

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OfferGlobe is an offshore advertising company with multiple registered addressees both in the UK and seemingly in the tax haven of Seychelles.

They provide zero customers support, nor any real world address. Additionally, they seem to have no real employees except a guy out of the UK called “Steve Mandes” who refused to answer questions about his company.  

The name may be a pseudonym for someone else in the industry using “OfferGlobe” as a scam. His facebook profile has no personal photos or any personal information. Additionally, he claims he is not the “owner” but just a VP. 

The company is engaged in offshore marketing in violation of the FTC, and does illegal spam calls to mobile phone and land lines for bankruptcy and lender scams.

A Contact with the FTC has said they have received numerous complaints but are unable to track down the offshore scammers. This seems to be purposely done, so they are not prosecuted or sued.

Additionally, they sell data that is not COPPA complaint, nor follow local and state laws including California Privacy laws. Their Privacy and Tracking Policy does not have an address, nor any contact information making their collection of data potentially illegal.

We can not recommend anyone do business with a company that purposely hides who owns their company, and worse, is offshore.

What Marketers Must Know About CBD Ads

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An increasing number of celebrities and social media personalities are endorsing the use of cannabidiol (CBD) products through social media. Many of these “influencers,” however, fail to take into account and comply with the complex regulatory environment surrounding CBD advertisements, which can have consequences for CBD companies themselves. In the United States, the Federal Trade Commission (FTC) and the Food and Drug Administration (FDA) both limit the use of certain language in CBD endorsements. As these advertisements attempt to reach the broadest possible audience, possible violations are especially noticeable to regulators, who have stepped up their enforcement efforts in this area.

What is CBD?

With the passage of the 2018 U.S. Farm Bill, hemp-based CBD products were removed from the Drug Enforcement Administration’s list of scheduled substances, thereby decriminalizing the possession of such CBD products. The Farm Bill defines hemp as a strain of the Cannabis sativa plant species that does not contain more than 0.3% of the psychoactive component tetrahydrocannabinol (THC). Instead, hemp has significantly higher concentrations of CBD. The legalization of recreational and medicinal marijuana in certain states refers to the cannabis plant containing high levels of THC, which may also contain some CBD. Certain states, such as California, have stringent requirements regarding advertising cannabis products, but these rules do not apply to hemp-based CBD products.

Direct versus Affiliate Marketing

Advertising through social media falls into two broad categories: direct advertisements and affiliate marketing. Direct advertisements are paid by the company to appear in a customer’s feed with the term “Advertisement” somewhere in the post. These direct advertisements are most similar to traditional commercials in other forms of media. Affiliate marketing, which is the centerpiece of this article, occurs when an influencer earns a commission for referring his or her followers to a brand or site. These referrals usually happen through affiliate links (e.g. brand.com/influencer) or promotional codes (e.g. typing “Influencer Name” as a promotional code during checkout).

Social Media Giants: The Main Affiliate Marketing Platforms

Social media companies have disparate views regarding the ability to promote CBD products on their platforms in the United States. The two main social media giants are the primary websites celebrities and influencers use to promote products. Other social media platforms, such as Twitter, allow direct advertisements for CBD products. However, more CBD companies use affiliate marketing through these social media giants than direct advertisements.

Despite not having explicit rules against direct advertisements for CBD products, the primary social media platforms have repeatedly taken down such advertisements. As a result of these practices by these social media platforms, influencers have gained prominence as a method for CBD companies to improve traction in the increasingly-crowded space. With influencers earning up to $50,000 for a single sponsored post, affiliate marketing provides influencers with a lucrative business opportunity and CBD companies with a method to reach millions of people. As sponsored posts become more prevalent, the FTC and FDA have taken more of an interest to regulate advertising infractions.

CBD Advertising Regulations: The FTC and FDA

The FTC and FDA are leading the federal regulation of CBD products and advertising, and the agencies collaborate to prevent unlawful activity, including through social media platforms.

FTC

In 2009, the FTC issued guidelines concerning the use of endorsements and testimonials, which seek to prevent companies from using these marketing tools to circumvent advertising laws. In addition to providing detailed examples, the guidelines state that if paid testimonials or endorsements are false or misleading, the company itself can be held responsible. Additionally, all cases of a “material connection,” including paid relationships and free products, between the endorser and advertiser must be “clearly and conspicuously” disclosed in the sponsored post. For example, an influencer promoting a product must state the disclosure without the viewer needing to click “more” in the caption. In 2017, the FTC provided updated FAQs regarding such disclosures and other endorsement claims.

In more recent news, the FTC filed its first lawsuit involving COVID-19 related claims. The FTC sought injunctive relief in federal court and simultaneously filed an administrative action against a defendant who had marketed its CBD products as able to treat and prevent COVID-19. The defendant had also been the recipient of a warning letter from the FDA regarding illegal marketing of its CBD products. This lawsuit demonstrates the FTC’s ability to quickly investigate and respond to unsubstantiated health claims and as discussed further below, the FTC will act swiftly for egregious CBD advertisements. FTC Commissioners have made clear that deceptive influencer marketing is a top priority for the agency.

FDA

Congress specifically preserved the FDA’s authority to regulate products containing CBD under the Federal Food, Drug, and Cosmetic Act (FD&C Act) and Section 351 of the Public Health Service Act. One of the FDA’s main concerns is the “proliferation of egregious medical claims being made about products asserting to contain CBD that haven’t been approved by the FDA.”

The FDA also has significant safety concerns regarding the use of CBD in foods and dietary supplements due to potential liver damage issues. Because of the FDA’s approval of an anti‑seizure medication called Epidiolex® and the substantial clinical trials related to Sativex®, the FDA’s present position is that CBD products cannot be marketed as food or dietary supplements. In its recent report to Congress, the FDA has specifically indicated the questionable safety of CBD products and contemplated whether they meet the necessary safety standards to market CBD as a food or dietary ingredient. The FDA has stated that it has not received sufficient information to confirm that CBD meets this standard. With that said, the FDA has generally used its discretion enforcing these restrictions in regard to the CBD products on the market as long as the products do not contain claims about the treatment of diseases, as described in further detail below.

The FDA has an entire webpage dedicated to regulatory resources, FDA communications, and FAQs regarding the use of CBD in various products. The FDA has previously suggested it is open to developing a regulatory framework if it can be shown that CBD meets the regulatory standards. Given its recent report to Congress, it is unlikely anything will be released in the near future.

Last year, the FTC and FDA sent joint warning letters to CBD companies that claimed their products could treat Alzheimer’s, cancer, and other serious diseases. The agencies asserted that the touted health benefits were unsubstantiated health and efficacy claims and that, given these claims, the products at issue would fall under the classification of a “drug” under the FDA’s statutes. A few of the companies that received the warning letters had attempted to categorize the CBD products as “dietary supplements,” which would preclude them from categorization as a drug and related regulation, but the FDA concluded that CBD products are excluded from the definition of a “dietary supplement.”

The FDA has indicated that its enforcement actions will focus on situations in which a product developer makes unproven claims to treat serious diseases, as “patients may be misled to forgo otherwise effective, available therapy and opt instead for a product that has no proven value or may cause them serious harm.” With that said, the FDA has also stated the addition of CBD to cosmetic products is lawful. These products, however, cannot make claims that the product cure, treat, or prevent any disease or health-related condition, including aches and pains which are classified as topical external analgesic drug products.

Drafting or Reviewing Social Media Posts

Due to the regulatory issues surrounding CBD advertisements, CBD companies should include in their influencer contracts that the company has the right to review, or even write, the social media post. Profile posts, rather than disappearing stories, are the easiest to review, since the CBD company has plenty of time to review prior to publication. Although the disappearing stories can be saved to the influencer’s profile, profile posts allow for a scripted statement and therefore reduces the risk of unintended language.

How to Advertise CBD Products: Tips for Influencers and CBD Companies

Below is a quick list of practical tips for both influencers and CBD companies when entering into a CBD affiliate marketing contract:

Celebrities/Influencers

  • Do not state that the CBD product could treat, mitigate, cure, or prevent diseases, including aches and pains.
  • Do not state that CBD products are lawfully marketed in all 50 states. For instance, powerful lobbying groups have successfully stalled legislation in California regarding CBD.
  • Work with the CBD company to preview the post prior to publication or receive help writing the post.
  • Review the FTC’s Endorsement Guides and FAQs describing disclosure rules and examples of properly promoting products through social media.
  • If receiving a free product or payment for a sponsored post, ensure such disclosure is “clear and conspicuous.”

CBD Companies

  • Contract for specific language to write or review the influencer’s post prior to publication.
  • Utilize posts, rather than disappearing stories, to ease review and to reduce the influencer’s ability to go “off-script” during a live broadcast.
  • Be aware of the Consumer Review Fairness Act, which prohibits companies from using contract provisions to restrict consumers’ ability to honestly review products and services or to threaten or penalize consumers for posting negative reviews or complaints, including through affiliate marketing in social media platforms.
  • Be aware that advertisements for subscription or auto-renewal programs face an additional level of scrutiny. Subscription programs must provide additional disclosures, including clear information that the customer is enrolling in an auto-renewing program.

The passage of the 2018 U.S. Farm Bill decriminalized hemp-based CBD, which has led to an influx of CBD products. As CBD companies are prohibited from direct advertising through many social media and traditional marketing platforms, an increasing number of them are turning to celebrities and social media influencers for affiliate advertising. Given the risk to marketers, companies should avoid working with an influencer that does not follow the regulations and guidelines. With the CBD market expected to grow up to $23 billion in 2023, CBD companies will increasingly look towards influencers as a way to promote their products. The FTC and FDA have increased their focus and scrutiny towards influencer marketing and CBD advertisements, so both CBD companies and influencers need to fully understand the CBD advertising rules and regulations.

Affiliate Scammers Michael Giannulis and Michael Williams Named by Feds for $300 Million in Fraud

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The FTC Building

The Federal Trade Commission (FTC) cracked down a group of affiliate marketers who ensnared consumers into a fraud business coaching program called My Online Business Education (MOBE).

On Thursday, the FTC announced that charges have been filed against the affiliate marketers namely Michael Giannulis and Michael Williams along with their companies BPO USA LLC, Pixx Media LLC, and MyEcomClub Express.

In the complaint, the Commission alleged that the defendants sold to consumers worthless membership packages from MOBE. The defendant’s sales agents who purported to be business coaches claimed that they could teach consumers how to start and grow their online business to make a substantial income.

The consumers deceived by the defendants paid thousands of dollars for the online business coaching scheme. Giannulis and Williams through their companies bilked more than $30 million from their victims.

The Commission also filed complaints against Steven Bransfield and his companies SB & A Media, SB&A Group, and Werunads; Gar Leong Chow and his company TTZ Media, and Scott Zuckman and his firm Alpha Quad Enterprises.

In the lawsuit, the SEC alleged that the defendants operated high-ranking affiliates of the MOBE scheme. Since 2013, they lured tens of thousands of consumers and defrauded them more than $300 million.

MOBE victims suffered substantial losses, experienced crippling debts
The consumers who purchased the MOBE’s online business coaching program “suffered devastating financial losses or crippling debt” contrary to the affiliate marketer’s claim that they would generate significant income, according to the FTC.

In a statement, FTC Bureau of Consumer Protection Director Andrew Smith said, “These so-called ‘affiliates’ helped MOBE swindle consumers out of millions of dollars by making outlandish and false earnings claims. Affiliates should take note that the FTC will hold you personally and financially accountable for false or unsubstantiated marketing claims.”

Affiliate marketers agreed to settle FTC charges
The defendants agreed to pay FTC a monetary judgment to settle the charges against them.

Defendant Chow and TTZ Media accepted the Commission’s order requiring him to pay $3.35 million in monetary judgment.

On the other hand, Giannulis, Williams and their companies agreed to the FTC order requiring them to a $31.6 million monetary judgment, which will be suspended once they pay $760,000 and turnover personal items obtained from their participation in MOBE.

Meanwhile, Bransfield and his companies consented to the FTC order imposing a $4.7 million monetary judgment, which was suspended due to their inability to pay. In August 2019, the defendants filed for Chapter 11 bankruptcy.

Defendant Zuckman and his company agreed to the Commission’s order requiring a monetary judgment of $1.8 million, which will be suspended upon his payment of $406, 150. The suspension of the monetary judgment was due to the defendant’s inability to pay.

All of the settling defendants also agreed to permanently stop selling or marketing any business coaching program and money-making method.

In February, the primary culprits behind MOBE agreed to pay more than $17 million to settle the FTC’s lawsuit.

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How to Narrow the Scope of Information Sought by an FTC Civil Investigative Demand (CID)

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A civil investigative demand (“CID”) is the instrument by which the Federal Trade Commission exercises its compulsory process authority in connection with investigations.  CIDs may require the production of documents - including electronically stored information – or tangible things, the provision of testimony, and the providing of written responses to questions. A CID must state the nature of the conduct constituting the alleged violation which is under investigation and the provision of law applicable to...

Did Your Company Receive a Letter From the FTC?  FTC Warning Letters and Notices of Penalty Offense

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Recipients of FTC warning letters and notices of penalty offense should be on high alert and act quickly. Their advertising and marketing practices could be in violation of applicable legal regulations. What is an FTC Warning Letter? Federal Trade Commission “warning letters” are intended to warn companies that their conduct is likely unlawful and that they can face serious legal consequences, such as a federal investigation or lawsuit, if they do not immediately stop. ...

The Good, the Bad, and the SPO-ly

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The Hidden Flaws Behind Ad Tech’s Favorite Buzzword. Supply Path Optimization (SPO) is my love-hate relationship in ad tech personified. It’s the reason I fell for this industry’s maddening brilliance—and why it sometimes feels like a bad rom-com where no one learns their lesson. At its core, SPO promises efficiency, transparency, and accountability, and when it works, it’s like watching a Rube Goldberg machine perform flawlessly. But when it doesn’t—and let’s be honest, that’s most...