1. What are the four ways to sell supplements?

They differ by who holds the stock and who holds the risk, and that decides everything else.

Model Who holds stock Margin shape Where it breaks
Buy wholesale, sell from the shelf The clinic Best of the four — you keep the whole spread Capital in inventory, expiry dates, and a sales-tax obligation in most states. Dead stock is the usual way this loses money.
Dropship under your own brand or label The supplier Lower than shelf, no capital tied up You own the customer experience for a shipment you do not control. Returns and delays are yours.
Third-party dispensing platform The platform A set share, usually the smallest The account and the patient list may belong to the platform rather than to you. Ask what happens to both if you leave.
Recommend only, no sale Nobody None Removes the conflict entirely and removes the revenue with it. A legitimate choice, and some practices make it deliberately.

The question to settle before the model: is this a retail line or part of a protocol? A retail line is priced like retail and lives near the front desk. A protocol component is ordered, recorded and reviewed like anything else in the plan — and it is the second one that has to appear in the chart.

2. What do you actually need to sell them?

Less than people expect federally, and more than people expect locally. Dietary supplements sit under the Dietary Supplement Health and Education Act of 1994, enforced by the FDA with the FTC covering the advertising. Under that framework the manufacturer — not the clinic reselling — carries responsibility for safety and labelling.

Requirement Where it comes from Practical version
A business licence State and local The ordinary one you already hold to operate. Selling product may add a local permit.
A seller’s permit State Needed to collect and remit sales tax when selling to consumers.
A resale certificate State What lets you buy wholesale without paying tax at purchase, because the tax is collected at the sale instead.
Sales tax on the supplement itself ⚠️ State — and it differs Some states tax supplements as ordinary retail. Some exempt them when dispensed or prescribed by a licensed practitioner, which is a different answer for the same bottle depending on who hands it over. Check yours before the price list.
No FDA approval of the product Federal (DSHEA) Supplements are not approved before sale. That is the framework, not a loophole — and it is why what you say about them is where the risk lives.

3. What you can and cannot say about them

This is the part that creates real exposure, and it is free to get right. A supplement may carry a structure/function claim — what it does in the body — and may not carry a disease claim. The moment a product is described as treating, preventing or curing a condition, it is being marketed as a drug.

Safe shape The line you are crossing
“Supports healthy inflammatory balance.” “Reduces arthritis pain.” — a disease claim.
“Helps maintain normal blood glucose already in the normal range.” “Treats insulin resistance.” — a disease claim.
“Supports restful sleep.” “Cures insomnia.” — a disease claim.

⚠️ This applies to your words, not just the label: the shelf talker, the website copy, the protocol PDF and what a staff member says at the desk are all marketing. The FTC standard is substantiation — you need support for what you claim, and enthusiasm is not support.

4. The disclosure that protects you

Selling a product you also recommend is a conflict of interest. It is not prohibited; it is disclosed. The standard practitioner disclosure has four moving parts, and it is worth using something close to it verbatim:

Part What it says
The markup That the practice sells supplements at a stated percentage above cost.
The comparison What that still represents against ordinary retail, if it does.
No obligation That the patient may buy the same products elsewhere.
Care is unaffected ⭐ That their quality of care does not change either way. This is the sentence that matters, and it has to be true.

Where it belongs: in the consent or programme paperwork, on the shelf, and on the receipt. A disclosure buried in a policy binder is not one.

5. What the chart has to record when a bottle leaves the shelf

If it was part of the plan, it belongs in the record — not only on a receipt. The failure is always the same shape: a patient is taking something nobody wrote down, and it turns up for the first time during a medication reconciliation or a reaction.

Field Why
Product, strength and form Two bottles with the same name are routinely different doses.
Lot and expiry The same reason as any other stock: a recall is answered with a query, not a memory.
Quantity and date Makes an adherence conversation possible at the next visit.
Who handed it over, and under whose plan ⛔ A supplement dispensed by a staff member belongs on that clinic’s own list, never attributed to a clinician who did not order it.
It appears in the medication list Interactions do not care that something was bought at the front desk.

And the stock side: count moves at the dispense, not at the order. Deducting when a box is ordered is how the shelf and the system quietly diverge until something runs out mid-clinic.

6. What it is actually worth

Enough to matter, not enough to build a clinic on. The honest framing: supplements are a service the patients already want — most of them are buying something, somewhere, with no clinical oversight at all — and margin is the reward for doing it properly rather than the reason to do it.

Reality What follows
Shelf stock ties up capital and expires Carry a short list deeply rather than a long list thinly. Ten products that move beat forty that do not.
The best seller is the one inside a protocol Anything not attached to a plan sells like ordinary retail, which is a business you are not set up to win.
Refills are the whole economics A first bottle is a sale; the fourth is a programme. That is a reminder-and-reorder problem, and it belongs in the software.
⚠️ A markup you would not say out loud is the wrong markup The disclosure above has to be one you are comfortable handing to the patient.

7. Frequently asked questions

Do I need a licence to sell supplements in my clinic?
Federally, no product approval is involved — supplements sit under DSHEA and the manufacturer carries responsibility for safety and labelling. Locally you generally need your ordinary business licence, a seller’s permit to collect sales tax, and a resale certificate to buy wholesale. Some states add permits of their own, so the answer is your state’s, not the internet’s.

Is sales tax charged on supplements?
It depends on the state, and in several states it depends on who dispenses them — some exempt supplements when they are dispensed or prescribed by a licensed practitioner while taxing the same bottle sold at retail. Settle it before you set prices, because it is the difference between a margin and a shortfall.

Can I say a supplement treats a condition?
No. A dietary supplement can carry a structure/function claim about how it works in the body; describing it as treating, preventing or curing a disease markets it as a drug. That applies to your own copy, your shelf signage and what staff say, not just the manufacturer’s label.

Is it a conflict of interest to sell what I recommend?
It is, and the answer is disclosure rather than avoidance: state the markup, say the patient can buy elsewhere, and say plainly that their care does not change either way. Put it in the paperwork and on the receipt.

Does a dispensed supplement belong in the chart?
If it is part of the plan, yes — product, strength, lot, quantity, date, who dispensed it, and on the medication list. A receipt is a record of a sale. Interactions and reconciliation need a clinical record.