The pack says it is tested, but names no lab or certifier.
A testing badge without an issuer or report is a marketing claim, not evidence. Ask for the lab name and lot-specific report.

The pack says it is tested, but names no lab or certifier.
Rebuilt from public sources on July 23, 2026 · evidence availability is not a safety or effectiveness verdict.
A testing badge without an issuer or report is a marketing claim, not evidence. Ask for the lab name and lot-specific report.
This is category history, not proof about this product, but it changes how much unsupported claims deserve to be trusted.
Only product facts and comparisons earn a card. Pipeline gaps stay collapsed.
The listing claims third-party testing without naming any lab or certifier, so the claim can't be verified as stated.
Why it mattersA testing badge without an issuer or report is a marketing claim, not evidence. Ask for the lab name and lot-specific report.
Open the source-linked findingFDA's health-fraud program documents sexual-enhancement products as the most common supplement category found to contain undeclared prescription-drug ingredients. This is a category-level documented fact from FDA's public database — not a test result for this specific product. So…
Why it mattersThis is category history, not proof about this product, but it changes how much unsupported claims deserve to be trusted.
Open the source-linked findingThese are evidence gaps, not strikes against the product.
Can the testing claim be tied to a named laboratory and this product lot? Evidence that would settle it: lot-specific COA naming the laboratory and matching the product lot.
Confirmed evidence
These checks found support in the public record. They confirm specific facts, not the product as a whole.
Nothing could be independently confirmed from the available record.
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, unit count, 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.
The listing claims third-party testing without naming any lab or certifier, so the claim can't be verified as stated.
Open Food Facts resolves 039442030320 to "Test" (brand not supplied), but that record lacks enough exact brand/product detail to confirm or contradict this listing.
FDA's health-fraud program documents sexual-enhancement products as the most common supplement category found to contain undeclared prescription-drug ingredients. This is a category-level documented fact from FDA's public database — not a test result for this specific product. Source: fda.gov (linked in Related research).
The NIH Dietary Supplement Label Database has no matching label yet. Ingestion lags the market — recorded as a gap, not a strike.
This means only that no enforcement record matched the brand name — it does not mean the product was tested, reviewed, or cleared by FDA. New and untested products also have no recall records.
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 310 on 2026-01-28 to 319 on 2026-07-18 (net +9). 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
Can you send the certificate of analysis (COA) for the lot number on my bottle?
A real COA names the testing laboratory, the test date, the lot it covers, and what was measured. “Third-party tested” with no document behind it is a marketing sentence.
Can you send a clear photo of the full Supplement Facts panel?
It’s the one part of the label required to state what’s inside and how much. A seller who won’t show it before purchase is asking for trust the label would have earned.
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
Scan the barcode on the package and confirm it reads 039442030320.
A mismatch between the barcode on the box and the one on the listing is worth pausing over — it can indicate a different variant, a repack, or a counterfeit.
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 23, 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.