
FDA-registered facility
The factory is listed with the FDA. It does not mean the FDA approved this product, and the FDA does not approve supplements before they are sold.
Four marks shown with this product, and not one of them is a test result. Here is what each covers and what it does not.
Horse Mood is shown with an FDA-registered facility roundel, a GMP mark, a foreign-and-domestic-ingredients seal and a money-back satisfaction badge. All of these describe the factory, the paperwork or the marketing, not the capsule. None is an FDA approval, because the FDA does not approve dietary supplements before they are sold, and no laboratory test report for this product was published to us.
These are the marks supplied with the product. The reads beside them are ours.

The factory is listed with the FDA. It does not mean the FDA approved this product, and the FDA does not approve supplements before they are sold.

Good Manufacturing Practice. Rules for how a product is made, recorded and traced, not for whether it works or whether any amount inside a blend is adequate.

An unusually honest seal: it says outright that the ingredients come from more than one country, rather than implying everything is grown here.

A marketing badge. No seller money-back window was published to us, and the only return route we can confirm is the one on the marketplace listing.
“Manufactured in an FDA-registered facility” sounds like approval and is not. Registration means the factory has told the FDA it exists and is on a list. Any facility making food or supplements for sale in the US has to do it, and it says nothing about the product made there.
The FDA is explicit about this. Its own consumer guidance states that it does not have the authority to approve dietary supplements before they are marketed. There is no pre-market review of a supplement's formula, its claims or its safety.
That is why you will not find the words “FDA approved” anywhere on this website. Not about this product, not about any product. Where a seller uses them, it is either an error or a claim US law does not support.
What the FDA can do is act afterwards: inspect facilities, issue warning letters and require recalls. The responsibility for a supplement being safe and accurately labelled sits with the company selling it, before and after it reaches a shelf.
Made in an FDA-registered facility. Nothing more than that, and it is worth knowing that a registration is an address on a list rather than a verdict on a capsule.
| Mark | What it covers | What it does not cover |
|---|---|---|
| FDA-registered facility | The factory is listed with the FDA and subject to inspection | The formula, the claims, the doses, or whether the product works. There is no pre-market approval of a dietary supplement. |
| GMP (Good Manufacturing Practice) | How the product is made, documented, cleaned and traced | Whether any ingredient helps with anything, and whether any amount is adequate. A GMP facility can make an undisclosed blend perfectly. |
| Foreign and domestic ingredients | That raw materials come from more than one country | Which ingredient came from where. It is unusually candid for a seal and still not specific. |
| Money-back satisfaction badge | Nothing verifiable | No seller money-back window was published to us. The only return route we can confirm is the one printed on the marketplace listing. |
Four marks, and none of them touches the contents of the capsule. This is not unusual, and it is worth knowing before a seal on a product page does any work in your decision.
Three documents would change this page, and none of them was published to us.
A breakdown of the blend. This is the specific document this product needs, because the panel prints one number for eight ingredients. A single page splitting 1,200 mg into eight figures would answer nearly every open question on this site, and it would cost the manufacturer nothing but the decision to publish it.
A certificate of analysis for the batch, naming the laboratory and printing results against specifications. We have a certificate reference, HOR-6587-26-TH, and no certificate.
A heavy-metals and microbial screen. Any product built from dried botanical material carries that question, and this one is seven botanicals plus bovine tissue.
We asked for all three. We print what we were given, and what we were not. If any of it is published later, it goes on this page with the date it arrived.
The full list, not only the testing items.
This bottle carries no “Distributed by” line at all, which is unusual enough to be worth stating plainly. The only company name anywhere on it is the brand line Vitalifes, printed above the product name on the front, with no address, no phone number and no website beside it. Neither a manufacturer nor a distributor was published to us.
This product carries the reference HOR-6587-26-TH, and no document behind it was published to us. A reference number is a pointer; a certificate of analysis is a laboratory document that names the lab, the test dates, the specifications and the results. The gap between the two is exactly the gap between saying a thing was tested and showing that it was.
On most supplement labels, a buyer who wants the certificate of analysis has somewhere to send the request. The distributor is printed on the bottle, with an address, and often a website.
This bottle has none of that. There is no “Distributed by” line anywhere on it. The only company name is the brand line Vitalifes, printed above the product name on the front, with no address, no phone number and no website beside it.
That is unusual and it is worth naming plainly, because it closes the one route a diligent buyer would otherwise have. The order desk on +1 (302) 200-3480 handles orders and refunds; it is not the manufacturer and does not hold formulation records.
So on this product, the request for a breakdown of the blend has no addressee. That is a different and worse position than a company declining to answer, because at least a declined request is an answer of a kind.
One bottle is 60 capsules: thirty days at two a day, sixty at one. Eight ingredients share a 1,200 mg blend, and the price is shown at checkout.
Order NowRead the label firstNo price was published to us. We print no figure we have not seen ourselves. · Returns run on the listing’s window · Not for pregnancy or nursingNo, and no dietary supplement is. The FDA states that it does not have the authority to approve dietary supplements before they are marketed. The roundel shown with this product says the factory is registered with the FDA, which is a requirement for any facility making food or supplements for sale in the US.
Not published. This bottle carries no “Distributed by” line at all. The only company name on it is the brand line Vitalifes, with no address, phone number or website.
Lot HOR-26/TH-6587, certificate reference HOR-6587-26-TH, expiry 07-2028. The certificate itself was not published to us, so the reference is all we can print.
No published safety study exists on this formula, and assessing an ingredient normally starts with its amount, which this panel does not publish. Nobody outside the manufacturer can tell you. Show the panel to your pharmacist.
Because the label uses a proprietary blend. Under 21 CFR 101.36(c) a blend declares the total weight of its dietary ingredients and lists them in descending order of weight; individual amounts are not required. It is legal, common here, and why no dose on this bottle can be checked.
One bottle is 60 capsules: thirty days at two a day, sixty at one. Eight ingredients share a 1,200 mg blend, and the price is shown at checkout.
Order NowRead the label firstNo price was published to us. We print no figure we have not seen ourselves. · Returns run on the listing’s window · Not for pregnancy or nursing