Quick answer
As of September 2026, the number of GLP-1 medicines with an FDA label that come as a skin patch is zero. FDA's openFDA label database counts 44 labels in the GLP-1 receptor agonist class with a subcutaneous route and 1 with an oral route, and none with a transdermal route. There is no "Ozempic patch": every semaglutide label describes an injection or a tablet. The products sold online as "GLP-1 patches" describe themselves as berberine or "wellness" patches, and both brands we read state that they are not a replacement for medication. Semaglutide is a peptide of about 4,114 daltons; the published rule of thumb for absorption through intact skin is a ceiling of 500 daltons. Compounded medications are not FDA-approved as final products.
Is there an Ozempic patch? What FDA's label database returns
Ozempic is Novo Nordisk's brand name for semaglutide injection. Its label on DailyMed (set id adec4fd2-6858-4c99-91d4-531f5f2a2d79) opens: "OZEMPIC (semaglutide) injection, for subcutaneous use, contains semaglutide, a human GLP-1 receptor agonist (or GLP-1 analog)." The first indication on its label is "as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus," and every indication it lists is in type 2 diabetes; weight management is an indication on the Wegovy label, not the Ozempic label.
openFDA answers with a count. Every semaglutide label by route: "SUBCUTANEOUS" 4, "ORAL" 1, nothing else (data last updated September 18, 2026). The whole GLP-1 receptor agonist class: 44 subcutaneous, 1 oral, no transdermal entry. Tirzepatide returns 8 subcutaneous labels, liraglutide 22, orforglipron 1 oral. The only brand names on a semaglutide label are Ozempic, Rybelsus and Wegovy. A product sold as an "Ozempic patch," or an "Ozempatch," the nickname Baptist Health reports from social media ads, is using the name, not the drug, and "Ozempic patch reviews" are reviews of a wellness patch that borrowed the name.
What a GLP-1 medicine is
GLP-1 receptor agonists are prescription medicines that copy a gut hormone; NIDDK describes semaglutide as a drug that "Mimics a hormone called GLP-1 that targets areas of the brain that regulate appetite and food intake." Tirzepatide also copies a second hormone, GIP. The longer version is in what a GLP-1 medication is. Two facts matter here: these medicines are peptides, which are large molecules, and every approved label carries the words "Rx only," which 21 U.S.C. 353(b)(4) requires on a prescription drug's label, so a licensed prescriber sits between you and the medicine.
Do GLP-1 patches really work? Why a stick-on patch cannot deliver a GLP-1 peptide
Skin is a barrier, and its outer layer is very good at keeping large molecules out. The most cited rule of thumb comes from a 2000 review in Experimental Dermatology: "We argue that the molecular weight (MW) of a compound must be under 500 Dalton to allow skin absorption. Larger molecules cannot pass the corneal layer."
Now the number for semaglutide. PubChem, the chemistry database of the U.S. National Library of Medicine, lists semaglutide (CID 56843331) with the molecular formula C187H291N45O59 and a molecular weight of 4114, more than eight times the 500 dalton ceiling. The same review notes that all known drugs used in transdermal delivery systems are under 500 daltons; a GLP-1 peptide is not.
That is also why the sellers changed ingredient. Cleveland Clinic reports that after backlash "some sellers have rebranded them as berberine patches." PubChem lists berberine (CID 2353) at a molecular weight of 336.4, small enough to clear the 500 dalton rule on paper. But berberine is not a GLP-1 receptor agonist, and the human evidence on berberine and body weight, including a 2026 systematic review in the International Journal of Obesity, is about berberine swallowed in randomized trials. Neither brand page we read cites a human study of berberine absorbed through skin.
Is a microneedle GLP-1 patch real? Research versus "microdart" listings
A 2008 review in Nature Biotechnology explains that large molecules such as insulin need microneedles or thermal ablation, then "progressing through clinical trials for delivery of macromolecules and vaccines." A July 2026 paper in AAPS PharmSciTech describes dissolving microneedles loaded with semaglutide and tested on porcine skin, and a 2024 paper in Advanced Therapeutics describes a microneedle patch designed for scheduled release of semaglutide. Both are preclinical; neither is a product with an FDA label.
Retail listings borrow the vocabulary. The Amazon search for "glp1 patches for weight loss" that we read on September 22, 2026 returned 185 results, among them products titled "Microdarts" and "Nano Patch." A listing that uses those words is not describing the published research unless it cites a study and a label; none we read does either.
Which brands sell GLP-1 patches in 2026, and what do their own pages say?
On September 22, 2026 we read three live product pages. Nothing here is a recommendation, and the review counts these pages display are not evidence of effect.
Kind Patches, "Berberine Patches (GLP-1 Friendly)." The page says: "Berberine Patches contain a blend of plant-based ingredients and essential nutrients presented in a format that cuts the friction in your daily routine." The panel lists berberine, pomegranate and cinnamon extracts, a vitamin B complex, L-glutamine and chromium, each with an amount per patch printed in milligrams or micrograms. Its FAQ answers the medication question directly: "Are Berberine Patches a replacement for medication? No. This product is designed to complement your routine, not replace medical treatment." On evidence: "The ingredients used in our patches are commonly included in wellness products and routines." As of September 2026 the page lists $15.00 for a one-time purchase and $12.75 on subscription. Its wear instructions are the seller's, not a label rule: "Use one patch at a time for up to 8 hours. Rotate patch location on your body with each use."
PatchAid, Berberine Patch. The URL that search engines indexed as a "GLP-1 support patch" now redirects to this page, which says: "This is a plant-based wellness patch. It does not contain prescription weight-loss or diabetes medications and is not a substitute for any prescription medication." Its panel lists berberine, pomegranate, cinnamon and gymnema extracts, B vitamins, L-glutamine and chromium picolinate, "with no caffeine or other stimulants on the panel." As of September 2026 a 30-day supply is $24.95. The site-wide footer: "PatchAid wellness patches are topical wellness products intended solely for general wellness and lifestyle support. They are not medical devices or dietary supplements."
Amazon, DlexoPel "GLPLUS-1 Berberine Patches." The title continues "20X Stronger with L Glutamine, Chromium, Pomegranate and Cinnamon, Multi-Part Body Application." Amazon prints its own disclaimer under the listing: "Statements regarding dietary supplements have not been evaluated by the FDA and are not intended to diagnose, treat, cure, or prevent any disease or health condition."
None of the three lists a GLP-1 receptor agonist, and two say in their own words that they are not a replacement for medication. One retailer files the product as a dietary supplement; one brand says its patches are not supplements at all, a disagreement the next section explains. The product is not the medicine the search phrase implies.
What is in a GLP-1 patch, and how to read the label
The berberine brands are one pattern. Baptist Health lists what other patches sold under the GLP-1 name contain: "Green tea extract Garcinia cambogia Bitter orange extract Vitamin B complex Guarana L-carnitine." Green tea, bitter orange and guarana are stimulant sources, which matters below.
Reading a patch label takes three rules. First, 21 CFR 101.36 requires a Supplement Facts panel on which "the names and the quantitative amounts by weight of each (b)(2)-dietary ingredient shall be presented under the heading 'Amount Per Serving'"; a "proprietary blend" with one total weight tells you less. Second, 21 CFR 101.93(c) fixes the disclaimer wording, "This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease," and FDA explains why: "because only a drug can legally make such a claim." Third, the statute defines a dietary supplement as a product that "is intended for ingestion" (21 U.S.C. 321(ff)(2)(A)(i)). A patch is worn, not swallowed, which is why PatchAid states that its patches are "not medical devices or dietary supplements," and why a patch can reach the market with no pre-market review under either pathway.
Last, the marketing words. "20X stronger," "GLP-1 friendly," "GLP-1 support," "nano" and "microdarts" are not regulated terms and appear in no label rule; "20X stronger" invites the question "twenty times what?" and the listing does not say. The category law in full is on our sister guide to stick-on weight loss patches.
How long do GLP-1 patches take to work, and do they work as well as injections?
The sellers answer the first question themselves. The Kind Patches FAQ recommends using the patches for at least three to six months and adds: "results can take time and may vary from person to person depending on factors like lifestyle, diet, or consistency." That is a wellness statement, not a clinical endpoint; a medicine with an FDA label states its indication, a wellness patch has none to state.
The second question has no head-to-head answer, because no study compares a wellness patch with a GLP-1 injection and none could: the patch does not contain the drug. Sharp HealthCare's article on shots, pills and patches makes the dose point: "The pills and patches marketed as supplements do not contain the same active ingredient. As a result, the exact dosage and potency of their ingredients are often unknown and inconsistent."
Are GLP-1 patches safe? Side effects, interactions and what FDA says
Start with the listings' own cautions. PatchAid: "Berberine may affect blood sugar and should not be combined with blood sugar medication without medical supervision. Not for use during pregnancy or nursing." Kind Patches: "Discontinue use if irritation or allergic reactions occur and consult a healthcare professional. Do not use if pregnant, nursing, or taking medication without consulting a healthcare professional." If you take a diabetes medicine, ask a physician before wearing a berberine patch.
Baptist Health lists the effects reported for the broader category: "Possible side effects of GLP-1 patches include: Skin irritation or rash Increased heart rate Jitteriness or anxiety Trouble sleeping Nausea Some ingredients act as stimulants and may raise blood pressure or interact with other medications." A Cleveland Clinic endocrinologist adds two risks of an unreviewed product: adulteration with unlisted ingredients, and an allergic reaction to the patch itself, "a condition known as contact dermatitis."
FDA's page "FDA's Concerns with Unapproved GLP-1 Drugs Used for Weight Loss," content current as of September 1, 2026, sets the frame: "This can be risky for patients, as unapproved versions do not undergo FDA's review for safety, effectiveness and quality before they are marketed." If a patch causes a reaction, FDA's MedWatch program takes the report: "MedWatch receives reports from the public and when appropriate, publishes safety alerts for FDA-regulated products."
What has the FTC done about weight-loss patches?
The Federal Trade Commission polices advertising, and on patches it has been specific for two decades. Claim seven in its Gut Check guide is the patch claim: "Weight loss is an internal metabolic process. Nothing you wear or apply to the skin can cause substantial weight loss. So weight loss claims for patches, creams, lotions, wraps, body belts, earrings, and the like are false." Its consumer article "The Truth Behind Weight Loss Ads" says the same in one line: "Lose weight with this patch or cream. (You can't.)"
The agency has enforced it. On August 20, 2007 the FTC announced that Transdermal Products International Marketing Corporation and William H. Newbauer were "banned from selling weight-loss patches in the future and will pay $180,000"; the advertising had claimed "that it caused weight loss and that the main ingredient, sea kelp, had been approved by the FDA for weight loss." On September 30, 2008 the marketers of the "Peel Away the Pounds" patch, Advanced Patch Technologies and Buckhead Marketing, "agreed to pay $110,539 to settle Federal Trade Commission charges that they violated two 2004 consent orders." These are historical cases about sea-kelp patches, not about any brand named here; the 2004 order that started them is on the weight loss patches page. The bar for any seller today is the FTC's Health Products Compliance Guidance: health claims "require substantiation in the form of competent and reliable scientific evidence."
Needle-free GLP-1 medicines that carry an FDA label
If the needle is why you searched for a patch, the FDA record contains oral options, all "Rx only" and all decided by a physician:
- Semaglutide tablets for weight management. The Wegovy label (set id ee06186f-2aa3-4990-a760-757579d8f77b) opens "WEGOVY (semaglutide) injection, for subcutaneous use WEGOVY (semaglutide) tablets, for oral use."
- Semaglutide tablets for type 2 diabetes. The Rybelsus and Ozempic tablets label (set id 27f15fac-7d98-4114-a2ec-92494a91da98) states: "RYBELSUS and OZEMPIC tablets, for oral use, contain semaglutide, a GLP-1 receptor agonist."
- Orforglipron tablets for weight management. Foundayo, from Eli Lilly (set id 8ac446c5-feba-474f-a103-23facb9b5c62), is an oral GLP-1 receptor agonist whose label says it "is indicated in combination with a reduced-calorie diet and increased physical activity to reduce excess body weight and maintain weight reduction long term in adults with obesity or adults with overweight in the presence of at least one weight-related comorbid condition."
The Zepbound label (set id 487cd7e7-434c-4925-99fa-aa80b1cc776b) reads "ZEPBOUND (tirzepatide) injection, for subcutaneous use." Which product, if any, fits a patient is a prescribing decision; our guides to oral tirzepatide, oral and sublingual GLP-1 forms and sublingual tirzepatide run the same label check on pills and under-the-tongue products.
Where compounded GLP-1 medicines fit
Compounding is a different category again. Under 21 U.S.C. 353a (section 503A of the Federal Food, Drug, and Cosmetic Act), a drug may be compounded "for an identified individual patient based on the receipt of a valid prescription order" by a licensed pharmacist in a state-licensed pharmacy. A prescription is the entry point; there is no over-the-counter compounded product.
FDA's Compounding and the FDA: Questions and Answers is direct: "Compounded drugs are not FDA-approved. This means that FDA does not verify the safety, effectiveness or quality of compounded drugs before they are marketed." Compounded medications are not FDA-approved as final products. For what that means in practice, read is compounded semaglutide FDA-approved and the difference between a 503A and a 503B pharmacy. A compounded GLP-1 is still a peptide, so the skin barrier applies to it too.
Checklist: is this a medicine or not?
- Look for "Rx only" on the label. Approved GLP-1 products carry it. A wellness patch carries "not intended to diagnose, treat, cure, or prevent any disease" instead. You cannot have both.
- Ask for the DailyMed set id, and read the route. Every approved drug label lives at dailymed.nlm.nih.gov with a permanent id, and for every GLP-1 receptor agonist its route reads subcutaneous or oral. No set id, no approved drug.
- Look for an NDC. FDA explains that drugs "are identified and reported using a unique, three-segment number called the NDC," and that inclusion in the directory "does not indicate that FDA has verified the information provided or that the products are FDA-approved," so treat the NDC as a starting point, not a seal.
- Check the prescriber's license. Every state medical board runs a public lookup; the Medical Board of California lists "profiles for all physicians and other allied health care providers who are licensed/registered in the state of California." See how to verify a doctor's license.
- Check the pharmacy's license. The Texas State Board of Pharmacy lets you "Verify a pharmacist, pharmacy (facility), and/or a pharmacy technician license/registration." A product that never names a pharmacy has nothing to look up.
- Read the label the way a pharmacist would. Drug name, strength, dosage form, prescriber, pharmacy, date; see how to read a prescription label.
- Read the terms before you pay. If the product is sold as a subscription, see what a GLP-1 telehealth subscription must tell you.
If a "GLP-1 patch" fails step 1, you can stop there. It is not a GLP-1 medicine, whatever else it may be.
Questions to ask a physician
Useful questions for a licensed physician:
- Which GLP-1 dosage forms exist with an FDA label today, and which, if any, fit my situation?
- Is anything in a wellness patch I already bought a problem with my other medicines, especially a diabetes medicine, and how do I report a reaction?
General questions about telehealth prescribing are answered in our help center.
This article is for informational purposes only and does not constitute medical advice. Medication is prescribed only if a licensed physician determines it is appropriate. Compounded medications are not FDA-approved as final products. Sources were read live on September 22, 2026; prices are as of September 2026 and change.
Frequently Asked Questions
Is there an Ozempic patch?
No. As of September 2026, openFDA lists every semaglutide label as a subcutaneous injection or an oral tablet, and the only brand names attached to semaglutide are Ozempic, Rybelsus and Wegovy. Ozempic is Novo Nordisk's injection; a product sold as an "Ozempic patch" is using the name, not the drug.
Do GLP-1 patches really work?
Not as a GLP-1 medicine. The listings we read on September 22, 2026 contain no GLP-1 receptor agonist, and the two brands' own FAQs say the patches are not a replacement for medication. A peptide of about 4,114 daltons does not cross intact skin, where the published rule of thumb is a 500 dalton ceiling.
Do the Kind Patches GLP-1 patches work?
The brand's own page answers this. Its product is titled "Berberine Patches (GLP-1 Friendly)," lists berberine, pomegranate, cinnamon, B vitamins, L-glutamine and chromium, and its FAQ says: "Are Berberine Patches a replacement for medication? No." On evidence it says the ingredients "are commonly included in wellness products and routines." It carries the standard disclaimer that it is not intended to diagnose, treat, cure or prevent any disease.
How long does it take for GLP-1 patches to work?
The sellers set their own expectation: the Kind Patches FAQ recommends at least three to six months and says results "can take time and may vary from person to person." There is no clinical endpoint because there is no drug; an approved medicine's label states its indication and trial design, a wellness patch has neither.
Do GLP-1 patches work as well as injections?
No comparison exists and none could be run, because the patches do not contain the drug. Sharp HealthCare's article makes the same point: the supplements "do not contain the same active ingredient."
Are GLP-1 patches FDA approved?
No GLP-1 patch has an FDA label. openFDA lists 44 subcutaneous and 1 oral label in the GLP-1 receptor agonist class and no transdermal route, and every patch page we read carries the "not intended to diagnose, treat, cure, or prevent any disease" disclaimer. A claim that a patch ingredient was "approved by the FDA" was the exact claim the FTC acted on in its 2007 sea-kelp patch order.
Are GLP-1 patches safe, and what are the side effects?
The listings' own cautions are the starting point: PatchAid says berberine "may affect blood sugar and should not be combined with blood sugar medication without medical supervision" and is not for pregnancy or nursing; Kind Patches says to stop if irritation or an allergic reaction occurs. Baptist Health lists skin irritation, increased heart rate, jitteriness, trouble sleeping and nausea for stimulant-containing patches. A reaction can be reported to FDA's MedWatch.
Which brands sell GLP-1 patches in 2026, and what do they cost?
As of September 2026, Kind Patches lists its Berberine Patches at $15.00, or $12.75 on subscription, and PatchAid lists a 30-day supply of its Berberine Patch at $24.95, both on their own pages. Amazon returned 185 results for the search, including DlexoPel GLPLUS-1. These are data points read on September 22, 2026, not recommendations, and prices change.
Can a compounding pharmacy make a GLP-1 patch?
No compounded GLP-1 patch carries an FDA label. Under section 503A of the Federal Food, Drug, and Cosmetic Act a drug is compounded only for an identified patient on a valid prescription, so there is no over-the-counter compounded product, and a compounded GLP-1 is still a peptide, so the skin barrier applies to it too. Compounded medications are not FDA-approved as final products.
What should I do if I had a reaction to a patch?
Stop using it, which is what the Kind Patches caution itself says, and contact a physician, especially if you take a diabetes medicine. A reaction can be reported to FDA's MedWatch program, which "receives reports from the public and when appropriate, publishes safety alerts for FDA-regulated products."
Is there any weight loss patch that works?
The FTC's Gut Check guide states that "Nothing you wear or apply to the skin can cause substantial weight loss," and no weight-loss patch of any kind carries an FDA label. The wider category, including the FTC's 2004 order, is covered in our guide to weight loss patches.
Sources
This article is based on the following primary sources. Links open the original documents.
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Majesta Health articles are written against primary sources (FDA labeling, NIH and CDC publications, state statutes) and each one passes a documented compliance review before publication. Where an article cites external sources, they are listed at the end of that article so you can check them yourself. No article currently carries an individual physician review; when a physician reviews an article, that page will show the reviewer's name, NPI and review date.
- Written against primary sources: FDA labeling and safety communications, NIH and CDC publications, state statutes and medical board rules
- Documented compliance review against FDA, FTC and LegitScript requirements before publication
- External sources, where an article cites them, are listed at the end of that article with links to the original documents
- Compounded medications are described as not FDA-approved as final products on every page that mentions them
