The panel states Potassium (from 550 mg Potassium Gluconate) 90 mg per serving.
Rebuilt from public sources on July 22, 2026 · evidence availability is not a safety or effectiveness verdict.
The panel gives a per-ingredient amount rather than hiding quantities inside a proprietary blend, so each one can be compared to published research.
Brand-level caution
Brand-level context only, not a finding about this product. Pharmavite recalled a different or not-exactly-bound product on 2016-06-06: “Specific lots of Nature Made(R) Vitamin D tablets may exceed specificatio…
The listing-image panel publishes an amount for each of its 1 declared row. That supports ingredient-by-ingredient review; it does not verify the contents.
| Panel row | Amount | %DV | What to notice |
|---|---|---|---|
| Potassium (from 550 mg Potassium Gluconate) | 90 mg | — |
FDA rules (21 CFR 101.36) require the amount of each dietary ingredient per serving unless hidden in a declared “proprietary blend” (legal, but a transparency yellow flag). A label stating no amount at all is non-compliant — a checkable red flag. This panel states amounts; the open question is whether those declared amounts are independently verified and how they compare with relevant research.
vision:google/gemini-flash-1.5 Amounts are shown as declared panel data, not independently lab-tested contents.
These are the USPTO records behind the brand name. We show them all rather than choosing one by similarity.
CALIFORNIA, USA · Registration 3520080
8531 Fallbrook Avenue, West Hills, CALIFORNIA 91304, UNITED STATES
IC 005: dietary supplements.
CALIFORNIA, USA; CALIFORNIA, USA · Registration 1963505
8510 BALBOA BLVD., NORTHRIDGE, CALIFORNIA 91325, UNITED STATES
IC 005: vitamins, minerals and dietary supplements.
This answers who owns registrations for the brand wordmark. It does not by itself prove which entity made, imported, or sold this specific product.
Review counts rose gradually. Written-review counts rose from 55 to 60 across the observed period. That describes count movement, not review authenticity or product quality. A variation family may share some public counts.
Keepa exact-listing history · counts do not prove authenticity · variation family may share counts
Which exact USPTO registrant is tied to this product's brand use? Evidence that would settle it: exact-wordmark ownership record.
Confirmed evidence
These checks found support in the public record. They confirm specific facts, not the product as a whole.
The panel gives a per-ingredient amount rather than hiding quantities inside a proprietary blend, so each one can be compared to published research.
Documented concerns
These are documented contradictions or claims that need more evidence. They are separate from missing data.
No contradictions or product-specific cautions were found at this check depth.
Unresolved public record
We looked for these signals but could not settle them from public sources. A gap is not a strike.
The retained listing evidence does not establish net weight, per-serving dose, servings per container, so the dose claim cannot yet be checked against serving arithmetic. This is a neutral evidence gap, not a pass or strike.
USPTO returned multiple live supplement-class records for the exact brand wordmark: PHARMAVITE LLC, PHARMAVITE CORPORATION. These records answer who owns registrations for the brand; the separate product-to-owner or manufacturer link remains open.
Brand-level context only, not a finding about this product. Pharmavite recalled a different or not-exactly-bound product on 2016-06-06: “Specific lots of Nature Made(R) Vitamin D tablets may exceed specifications for yeast/mold.” (status: Terminated). The recalled product was: “Nature Made(R) D3 1000IU, 125 count, UPC 0-31604-02793-3” — not necessarily the product on this page. Verify at FDA’s recall database.
The paid catalog links this exact item to a parent listing. Review counts on public product pages may be shared across sizes, flavors, or other variants, so the count history is listing context — not evidence that reviewers received or tested this exact variant.
Exact-listing history records written-review counts from 55 on 2026-03-20 to 60 on 2026-07-20 (net +5). Count movements can reflect sales, listing variants, collection resets, or moderation; this history does not establish whether reviews are authentic.
What to ask and check
Ask the brand or seller
What is the product’s UPC or GTIN?
The barcode is how a product gets matched to outside records — certification registries, label databases, recall data. Without it, almost nothing can be cross-checked.
Is this label filed with NIH’s Dietary Supplement Label Database (DSLD)?
Filing is voluntary, so absence proves nothing — but a filed label puts the full ingredient table on public record where anyone can read it.
Most brands and sellers publish a contact route. A clear answer adds evidence to the record; no answer leaves the question open.
Check for yourself — no one’s permission needed
Compare the panel on the bottle in your hand to the one shown in this record.
Ours was read from listing photos and can contain reading errors. The physical label is the source of truth — if they disagree, tell us and we’ll correct the record.
Check the lot number and expiry on the bottle against any COA you’re given.
A certificate that doesn’t name your lot doesn’t describe what you’re holding.
These are the open questions on this specific record — not a warning about the product, and not a suggestion to buy or avoid it. Getting them answered is how you decide for yourself.
Record built July 22, 2026. Sources: source listing observed at check time · USPTO Trademark Search · Keepa exact-listing history · NIH / published research · certification and regulator records where available. LookCloser publishes evidence and gaps; it does not advise for or against any supplement. Evidence-based corrections welcome.