How the Hell Is This Legal?
The 30-year-old loophole letting opioids and brain drugs pose as “dietary supplements.” Inside DSHEA’s failure and FDA’s powerless oversight.
Quick, plain-English investigations from Mothers Against Herbal Abuse (MAHA). Each story exposes how gas-station highs and unregulated “supplements” evade the law and endanger families.
The 30-year-old loophole letting opioids and brain drugs pose as “dietary supplements.” Inside DSHEA’s failure and FDA’s powerless oversight.
How Soviet-era pharmaceuticals like phenibut and bemitil slipped into U.S. vape shops disguised as stress-relief supplements.
The kratom Salmonella outbreak nobody wants to talk about. When “tested for fecal bacteria” becomes a marketing slogan, something’s gone wrong.
California became the first state to launch a full-scale crackdown on kratom and 7-hydroxymitragynine, showing how states can act now to protect families under existing consumer-safety laws.
DMAA, once sold as a “natural” extract, is an amphetamine-like stimulant repeatedly linked to cardiac arrest and death. Learn how it was banned, why it keeps reappearing, and what you can do to stop it.
Flavors, discounts, and neon displays are no accident. Vape retailers use Big Tobacco’s playbook to capture new teen customers. See the tactics and how to push back with MAHA tools.
Dabbing delivers extreme doses of THC through vaporized concentrates that can exceed 90 percent potency. Learn how to recognize the equipment, understand the risks, and talk to teens about the dangers of high-potency products.
Why the red-and-white “toadstool” is being sold as a legal high in gummies and chocolate despite the FDA’s 2024 statement that Amanita constituents aren’t approved for food. Includes the Paul Stamets/Joe Rogan clip and a link to MAHA Letters.
Multiple eighth-graders were hospitalized after kratom gummies on campus. Georgia’s 2023 KCPA set 21+ sales, but age limits aren’t enough. What happened, why “consumer protection” failed families, and how to press for a full ban using MAHA Letters.
Learn how to write short, powerful emails that move legislators to act. Based on the persuasion tactics of FDR, LBJ, and Ted Kennedy, this guide shows parents how to turn heart and credibility into real policy change.
Another round of kratom recalls exposes the same problem that started MAHA’s mission: fecal contamination and absent oversight. This follow-up revisits Upton Sinclair’s warning and asks why “natural” products still escape basic sanitation laws.
Colorful THC, kratom, and kava seltzers are being sold as “functional” drinks beside sodas. Learn how these psychoactive beverages target youth through candy-like branding and why MAHA calls for stronger retail age controls.
Virginia Beach’s student drug policy looks strict, but loopholes allow hemp, kratom, and “wellness” products to slip through. MAHA explains the fine print and shows how parents can help schools close the gaps.
Inside the September 24, 2024 “science” briefing that hid kratom’s 7-OH opioid chemistry, downplayed risk, and left lawmakers in the dark about what they were really legalizing.
A straight-talk guide to the yellow bottles and orange capsules promising “focus” and “brain boost” while quietly stacking unapproved stimulants and sedatives in doses no teenager should touch.
Gas-station highs aren’t loopholes — they’re already breaking the law. See how kratom, THC drinks, and phenibut products violate basic food-drug safety rules and what states can do today.
Section 781 of H.R. 5371 detonates the entire hemp loophole, banning Delta-8, THCA flower, HHC, THC-O, and every chemically converted intoxicant. A seismic shift in federal law that reshapes every vape shop and gas station in America.
A shocking investigation into high-stim powders sold on Amazon featuring yohimbine, rauwolfia, eria jarensis, and 400+ mg caffeine blends disguised as “fitness.” Teen athletes are the target — and the victims.
A MAHA predictive intelligence briefing identifying the next wave of “legal” opiate-like herbs and synthetic-natural hybrids: akuamma, picamilon, phenyl-GABA analogs, novel alkaloids, and the rise of “plant morphinics.”
A shocking look at arecoline vapes, chewable “buzz beads,” JUUL-style pods, and Zyn-like pouches made from areca nut — a WHO-recognized carcinogen now being marketed as a “stress reliever” and “legal buzz” to kids.
A plain-English parent briefing on akuamma, the new plant-based opioid-like drug being sold as “pain relief,” “relaxation,” and a “legal buzz” in vape shops — mirroring kratom’s rise step-for-step.
An essential breakdown of how federal and state Food, Drug, & Cosmetic laws define “adulterated” products — and how states can seize, embargo, and remove kratom, phenibut, and other gas-station drugs immediately.
A formal MAHA policy analysis examining how New York’s “consumer protection” approach conflicts with the state’s existing Food, Drug, and Cosmetic Act adulteration standards—and why regulation cannot cure illegality.
A sharp statutory critique of SB 994 showing how it bypasses Florida’s existing Chapter 499 protections, shifts oversight to the wrong agency, funds accommodation over enforcement, and creates a reactive system where compliance is tested after harm occurs.
When unapproved smoke-shop products injure or kill, families ask who is responsible—and discover no one can pay. This briefing exposes the liability loophole and proposes a simple fix: real financial responsibility.
A clear, parent-friendly guide to what happens when ADHD medications are mixed with kratom, 7-OH derivatives, phenibut/GABA products, high-caffeine shots, nootropic blends, and “legal mushroom” gummies.
UGLY documents real smoke and vape shop storefronts exactly as they appear—no filters, no commentary—to interrupt normalization and force communities to ask one simple question: Why is this here?
A primary-source MAHA Special publishing FOIA-obtained emails and attachments that document how industry lobbying coordinated travel, testimony, slide decks, and “science statements” to shape policy outcomes — in Congress, statehouses, and abroad.
An evidence-based overview of an opioid-acting drug sold as a supplement. This briefing explains its pharmacology, addiction and overdose risks, documented harms, and why regulators must act before harm escalates further.
A sharp policy critique showing how a state registry functioned as a government seal of approval for high-potency, dependence-friendly products — contradicting federal warnings and the state’s own food and drug laws.
A statutory explainer showing how Virginia’s 2026 nicotine law simply enforces long-standing FDA PMTA requirements, closes retail loopholes, and creates a clear, public legality test through the Attorney General’s directory.
A critical review of a January 2026 human tolerability trial now being cited to oppose regulation. This analysis shows how the study’s own data reveal toxicity signals, serious adverse events, and conflicts of interest that make it unsuitable as policy evidence.
A plain-language explainer of the FDA’s New Dietary Ingredient (NDI) process, what Johnson Foods submitted for a kratom product, why the FDA rejected that submission, and how federal enforcement gaps still allow rejected kratom products to remain on store shelves.
A MAHA policy analysis examining how readily kratom powder can be processed into drug-grade mitragynine and converted to far more potent opioid agonists. This briefing explains why ease of extraction, single-step conversion, and normalized industry methods support scheduling kratom powder as the appropriate upstream control.
A MAHA investigation into tetrahydropalmatine (L-THP/Corydalis), a dopamine-blocking psychoactive compound being sold as a supplement. This briefing explains its pharmacology, liver-injury signals, lack of FDA approval, and why it mirrors earlier unregulated drug failures.
An overview of how states are responding to rising recreational nitrous oxide misuse, which laws are closing retail loopholes, and why weak age-only restrictions continue to leave youth and communities exposed.
A plain-language breakdown of the Ohio Board of Pharmacy’s eight-factor analysis supporting Schedule I classification, explaining each statutory factor, the evidence relied on, and what the decision means for consumers.
Supplemental Reading is MAHA’s editorial arm — a weekly blog that pulls back the curtain on the unregulated side of the “herbal” supplement market. We unpack the policies, loopholes, and marketing tricks that keep dangerous chemicals on store shelves.
Every post connects to our main mission: educating lawmakers, parents, and communities about gas-station highs that masquerade as natural health products.
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