Explainer · 4 min read
What A Supplement Facts Panel Has To Say
Six names on a graphic and a panel on a bottle are not two versions of the same thing. One is a picture. The other is a document with rules.
A Supplement Facts panel must carry the serving size, the servings per container, and — this is the part that matters — the quantitative amount by weight of every dietary ingredient, printed immediately after its name.
A marketing graphic has no such rules. It can name six ingredients and stop, and that is exactly what HoneyPower’s does.
The practical difference: with a panel you can look up a published dose and compare. Without one you cannot start.
What the guide actually requires
FDA’s Dietary Supplement Labeling Guide is written as a list of questions. Three of them decide everything a buyer can learn from a bottle.
| Question | What it requires |
|---|---|
| Q3 | You must list the names and quantities of dietary ingredients present in your product, plus the serving size and the servings per container. |
| Q30 | You must list the quantitative amount by weight per serving immediately following the name of the dietary ingredient. |
| Q34 | A proprietary blend must be identified as one, with the total weight of all ‘other dietary ingredients’ contained in the blendon the same line, and its ingredients listed beneath it in descending order by weight. |
Note what Q34 concedes and what it still demands. A seller who does not want to publish six figures may publish one — but it must be a real total, and the order of the list then tells you which ingredient is the biggest and which is the smallest.
Why a graphic is not a substitute
HoneyPower’s listing graphic is a competent piece of design. Six tiles, six photographs, six names in clean type. It tells you the product contains honey, ginseng, maca, tribulus, horny goat weed and black pepper extract.
What it cannot tell you, because nothing requires it to, is whether the maca is 500 mg or 5 mg. Those are two completely different products and the graphic is identical for both.
A list of names tells you what to look up. A panel tells you whether looking it up was worth your time.
What the gap costs, in order
- You cannot compare to research. Every published dose is a number. Comparing needs two.
- You cannot assess an interaction. A pharmacist asked about black pepper extract will ask how much, and there is no answer.
- You cannot compare two products. Two bottles naming the same six ingredients could differ by a factor of a hundred.
- You cannot tell whether you are paying for ingredients or for a photograph of them.
The two-minute fix, which is yours not theirs
The panel exists. It is on the bottle, because it is required to be. The only thing that happened here is that nobody put a photograph of it in the material this site was given.
So the fix is mechanical: when the bottle arrives, turn it around, read the Amount Per Serving column, and write the six figures into the empty panel on this site’s home page. Two minutes, and you have the document the marketing did not give you.
Questions
Is it legal to sell a supplement without publishing the panel online?
Yes. The requirement is on the label, not on the advertising. A seller can market a product with a list of names and no amounts, and the panel on the bottle is where the quantities live.
Does a proprietary blend mean they are hiding something?
Not necessarily, and plenty of reputable products use one. It does mean you get one number instead of six, and the honest reading is that it protects a formula from being copied while also preventing a buyer from checking a dose. Both of those are true at once.
What if the bottle arrives and there is no panel at all?
Then something is wrong, and the order desk is the first call. A dietary supplement sold in the United States is required to carry one.
Sources
- Dietary Supplement Labeling Guide, Chapter IV: Nutrition LabelingU.S. Food and Drug AdministrationThe document this whole site is about, and the reason the absence of a panel matters. Question 30: “You must list the quantitative amount by weight per serving immediately following the name of the dietary ingredient.” Question 3: “You must list the names and quantities of dietary ingredients present in your product.” Question 34 covers proprietary blends, which must carry the total weight of the blend and list its ingredients in descending order by weight. The guidance is marked “Contains Nonbinding Recommendations.”
- FDA 101: Dietary SupplementsU.S. Food and Drug Administration“The FDA does NOT have the authority to approve dietary supplements for safety and effectiveness, or to approve their labeling, before the supplements are sold to the public.”
What this page was checked against
Every figure on it is transcribed from the supplied Supplement Facts panel and checked-out pack, derived by arithmetic from those, or taken from a source on the references page.