Price is public
Know the fee before sending files. No “contact sales” step and no hourly meter.
Independent label + listing screening
Find the mismatch before the marketplace does.
One documented review of your dietary-supplement label and Amazon listing. Fixed scope, fixed price, plain-English findings — without a sales call or an open-ended consulting quote.
From $49
3–5 U.S. business days
PDF evidence trail
No calls required
A clearer alternative
Built for a decision, not a consultation funnel.
Enterprise labs and law firms often start with a quote or a call. PanelCheckup starts with a published scope, a published price, and a defined deliverable.
Label + listing
The screen checks the PDF and the Amazon detail page together, where mismatches usually surface.
Evidence stays attached
Findings are organized into a dated PDF record with severity tags and recommended next steps.
Written by design
Send materials, receive a due date, and continue in email. A live call is never required.
Why screen before publishing
The cheapest correction is the one made before launch.
A pre-publication screen cannot eliminate regulatory or marketplace risk. It can give your team a dated, written record of the places most worth a second look before artwork, inventory, and listing copy are locked.
01
Artwork has to be revised lateA missed panel, warning, identity, or quantity detail can force another design and approval cycle.
02
The listing says more than the labelTitles, bullets, and images can drift from the current Supplement Facts panel or add claims the package does not make.
03
Verification prep starts with gapsMissing or inconsistent documents create avoidable back-and-forth when an ASIN receives a verification notice.
Policy context reviewed September 17, 2026: Amazon’s third-party verification process and its listing-to-panel review are separate workflows. Sellers receive ASIN-level notices, and approved testing providers submit verification documents directly. Source: Amazon Seller Central policy reference; policy mechanics summarized by Epstein Becker Green in SupplySide Supplement Journal (Jan. 28, 2026). PanelCheckup does not replace an approved testing provider.
Your label goes live on Amazon before an attorney ever sees it.
The cheapest moment to catch a claim problem is before you print and publish — not after a listing notice.
This is for you if:
- You are launching a new supplement label.
- You are changing claims, bullets, or images on an existing listing.
- You received an Amazon listing notice and want a written read of the label behind it.
If we miss your confirmed delivery date, you get a full refund — it is written in our Operating Terms, not a marketing promise.
View the $99 auditServices & pricing
Choose only the depth you need.
The turnaround clock starts after complete intake. Your confirmation email states a calendar due date in U.S. Eastern Time.
Teardown Teaser
$49A focused first pass on publicly visible label images.
Limited scope: label images only; excludes the 40-point audit, Amazon listing comparison, and revision/questions round.
- Top 2–3 potential issues
- One-page findings summary
- 3 U.S. business-day delivery
- Full credit toward a $99 audit within 14 days
Single-Label Audit
$99 Current launch priceThe core deliverable for one current label and one listing. Confirmed orders receive the displayed scope at the displayed price.
- 40-point advisory screen
- Listing-vs-label match check
- Plain-English PDF with severity tags
- 5 U.S. business-day delivery
- One revision round + 5 written questions
Amazon Verification Concierge
$149–$199Written preparation around Amazon’s third-party verification workflow.
- $149 for one ASIN
- $199 for up to 3 ASINs, or one ASIN plus alignment fixes
- TRF, testing-company and document checklists
- 5 U.S. business-day delivery
- No account access, lab testing or outcome promise
Optional protection after the one-time audit
The audit catches today’s gaps. LabelWatch watches what changes next.
You can stop after the one-time audit — monitoring is never required. It is built for brands whose ASIN stays live, because edits to bullets, images, A+ content, or marketplace rules can create new drift after a clean audit.
The practical choice: choose monthly when you want flexibility or are testing a listing. If the ASIN is expected to stay active for the next 12 months, annual is the lower-cost route: all 12 checks, one decision, and $69 saved.
What you are protecting: not a static label file, but the alignment between that label and the live Amazon listing over time. LabelWatch reviews one current label and one ASIN each month; it does not access your seller account, test product contents, certify compliance, or guarantee an Amazon outcome.
LabelWatch Monthly
$39/ month
Best for a short launch, test ASIN, or uncertain timeline. Cancel anytime.
- One label + one Amazon ASIN monitored
- Monthly listing-to-label comparison
- Written alert when material drift is found
- Monthly email summary and dated record
LabelWatch Annual
$399/ year
$468 at the monthly rate 12 checks for $69 less
- 12 scheduled monthly checks with no renewal gap
- One label + one Amazon ASIN monitored
- Written alerts and a year of dated records
- One payment — equivalent to $33.25/month
40-point review framework
A defined screen. No vague “expert review.”
Each report records what was checked, what was flagged, why it matters, and the next review step. The desk reviews documents only; it does not test product contents or certify compliance.
ASupplement Facts panelFormat, serving details, daily values, ingredient order
BClaim languageStructure/function wording, disclaimer presence, research flags
CAllergen statementsDeclared allergens and label consistency
DAmazon alignmentTitle, bullets, images, quantity and brand match
E–HWarnings & identityNet quantity, origin, business identity and cautions
View the full 40-point checklist
A. Statement of Identity
- Statement of identity appears as a principal feature on the principal display panel.21 CFR 101.3(a)
- Statement of identity includes “dietary supplement” or an allowed substitution.21 CFR 101.3(g)
- Statement of identity is bold, prominent, and reasonably sized.21 CFR 101.3(d)
B. Net Quantity of Contents
Note: older FDA labeling guidance cites this rule as 21 CFR 101.105 — the net-quantity rule was redesignated from 101.105 to 101.7 in 1986 (51 FR 25017); current 101.105 covers exemptions only.
- Net quantity declaration appears on the principal display panel.21 CFR 101.7(a)
- Discrete units are declared by count, not only by weight.21 CFR 101.7(a)
- Net quantity type size matches the principal display panel area.21 CFR 101.7(i)
- Net quantity appears in the lower 30% and contrasts with the background.21 CFR 101.7(f); 101.7(h)
C. Supplement Facts Panel
- “Supplement Facts” title is present, prominent, and bold.21 CFR 101.36(e)(1)
- Supplement Facts panel is enclosed by hairlines.21 CFR 101.36(e)(2)
- Panel typography follows style, color, case, leading, and spacing rules.21 CFR 101.36(e)(3)
- Panel type sizes meet the applicable standard, small-pack, or intermediate-pack minimums.21 CFR 101.36(e)(4), (i)(2)
- Serving size and servings per container are declared.21 CFR 101.36(b)
- Dietary ingredients with an RDI or DRV are listed separately with weights.21 CFR 101.36(b)(2), (c)
- Other dietary ingredients use the “Daily Value not established” symbol and footnote.21 CFR 101.36(c)
- Hairline rules separate (b)(2) and (b)(3) ingredients.21 CFR 101.36(e)(5)
- The 2,000-calorie Daily Value footnote appears when required.21 CFR 101.36(b)(2)(iii)(D)
D. Other Ingredients
- Other ingredients use common or usual names in descending order of predominance.21 CFR 101.4(a)(1); 101.36(g)
- Supplement Facts ingredients are not unnecessarily repeated in the ingredient list.21 CFR 101.4(a)(1) proviso
E. Name & Place of Business
- Name and place of business of the manufacturer, packer, or distributor appear on the label.21 CFR 101.5
- A qualifying phrase appears when the named business is not the manufacturer.21 CFR 101.5(c)
- Street address appears unless the directory-listing exemption applies.21 CFR 101.5(d)
F. DSHEA Disclaimer
- DSHEA disclaimer wording is exact and unmodified, using the correct singular or plural form.21 CFR 101.93(c)
- Disclaimer is adjacent to the claim or boxed on the same panel and linked to each claim.21 CFR 101.93(d)
- Disclaimer is bold and at least 1/16 inch in type size.21 CFR 101.93(e)
- Every structure/function claim carries the disclaimer on the label and in labeling.21 CFR 101.93
G. Structure/Function vs Disease Claims
- Claims describe structure/function or general well-being, not disease.21 CFR 101.93(f)
- Claims do not state or imply an effect on a disease, its signs or symptoms, or an abnormal condition.21 CFR 101.93(g)(2)(i)–(iv)
- Product-class terms do not imply disease treatment without structure/function context.FDA S/F Small Entity Guide, Criterion 5
- Claims do not present the product as a drug substitute or as having fewer drug side effects.FDA S/F Small Entity Guide, Criterion 6
- Client attestation is required for the 30-day FDA notification and claim substantiation.21 CFR 101.93(a)
H. Allergen Labeling
- Any of the nine major food allergens present are declared.21 USC 343(w)
- Allergen source is declared in a “Contains” statement or the ingredient list.21 USC 343(w) (FALCPA)
I. Prohibited & Misleading Content
- Label contains no false or misleading statement.21 USC 343(a) (misbranding)
- Label does not state or imply FDA approval or endorsement.General FDA principle
- Unauthorized disease claims receive a critical flag.21 CFR 101.93(f)
J. Amazon Listing Consistency
- Listing images and text align with physical-label claims and disclaimer placement.21 CFR 101.93(d) principle
- A+ content, bullet points, and image text contain no disease claim.21 CFR 101.93(g)
- Disease claims in listing testimonials or reviews receive a risk flag.Reported enforcement trend (CFR text nahi — report me “risk flag” ke tor par, verdict ke tor par nahi)
K. Legibility
- Required statements are conspicuous, legible, and not obscured by design elements.21 CFR 101.15 prominence
L. Scope Boundary
- Report states that product contents, formula accuracy, manufacturing/GMP compliance, substantiation dossiers, state laws, and FDA notification status were not verified.Scope boundary — no CFR citation
Illustrative report excerpt
See the work before you buy it.
Every finding answers three practical questions: what was observed, why it deserves attention, and what to do next. The excerpt is illustrative — not a client result and not a legal conclusion.
What if your label is already in good shape?
The report says that plainly. You still receive the completed checklist, dated evidence record, and any low-priority observations — not invented problems to justify the fee.
The report says that plainly. You still receive the completed checklist, dated evidence record, and any low-priority observations — not invented problems to justify the fee.
ILLUSTRATIVE EXCERPT · FINDING D22
Listing claim not found on current label
SEVERITY · MEDIUM
Listing claim not found on current label
Observed
The Amazon bullet uses a benefit statement that does not appear on the label PDF supplied for review.
Evidence recorded: current label version, listing URL, and the exact bullet text as of the report date.
Why it matters
The package and product-detail page are presenting different claim language. That inconsistency is worth resolving before the listing is treated as the current product record.
Next step
Confirm which wording is current. Then align the listing and label, or ask qualified U.S. regulatory counsel to review the claim before publication.
How ordering works
Four written steps. One dated deliverable.
01
Choose a service
Email hello@panelcheckup.com with the service name.
02
Send the complete intake
Attach the current label PDF, Amazon listing link, and answers to the five questions.
03
Receive a calendar due date
The clock begins only when the intake is complete. The confirmation states the delivery date in U.S. Eastern Time.
04
Receive the PDF by email
Your report arrives with the evidence record, severity tags, and recommended next steps.
Choose the right lane
Different options solve different problems.
PanelCheckup is not a replacement for counsel or laboratory verification. It is the fixed-scope document screen that can come before either.
Option
Price model
Process
Best for
Regulatory law firm
Quote, flat-fee estimate, or hourly work
Consultation-led; legal analysis available
Legal conclusions, representation, higher-risk claims
Testing / verification provider
Quote by product and testing scope
Approved-provider workflow and testing
Amazon verification submissions, cGMP and lab work
PanelCheckup
Fixed public price: $49 / $99 / $149–199
Written-only; no sales call; dated PDF
Early screening, label-to-listing alignment, verification prep
Comparison is category-level, not a claim about every provider. Research reviewed Eurofins and SGS label-review scopes, Lehrman Beverage Law’s consultation and review structure, and Amazon’s approved-provider process. Large providers commonly use quote-based scoping; PanelCheckup’s published pricing is the deliberate difference.
Operating terms
Clear before work begins.
Orders are handled asynchronously. No instant-response promise is required; the confirmed delivery date is the commitment.
U.S. business days
Monday–Friday, U.S. Eastern Time, excluding U.S. federal holidays. Capacity is capped at three active engagements. When full, new work is placed on a waitlist before intake.
Refunds & revisions
- Full refund if you cancel before work begins. Work begins when we start reviewing your intake documents.
- Full refund if delivery misses the confirmed date.
- No refund after an on-time completed report is delivered.
- One revision round within 14 days for the corrected version.
Unexpected disruption
If an event outside our control threatens the due date, we notify you before it passes. You choose either an extension of at least five U.S. business days or a full refund.
Questions before ordering
Clear answers, before you send a file.
If your question is not covered here, email it first. A question does not start the turnaround clock or commit you to an order.
Do I need a call?
No. Ordering, intake, questions, and delivery are handled in writing. This keeps the scope and evidence trail attached to the work.
What files should I send?
Send the current label as a readable PDF, the live Amazon listing link if applicable, and answers to the five intake questions. If the panel cannot be read at normal zoom, the intake is not complete.
What if no meaningful issue is found?
You receive the completed screen and a written record stating that no issue was flagged in the material reviewed, plus any low-priority observations. PanelCheckup does not manufacture findings to justify the fee.
What if I disagree with a finding?
The $99 audit includes one revision round and up to five written questions. You can provide context or a corrected label; the report will distinguish new evidence from the original observation.
Can PanelCheckup submit documents to Amazon?
No. We do not access seller accounts, contact Amazon, perform testing, or submit verification documents. The concierge prepares your written checklist and questions; an approved testing provider handles the verification submission.
When does the delivery clock begin?
Only after the current label PDF, listing link, and all five intake answers are received. Your confirmation email states a calendar due date in U.S. Eastern Time.
Important: this is not legal advice
PanelCheckup is a compliance research desk, not a law firm. Nothing in a report is legal advice, a legal determination, certification, or marketplace approval. Findings are advisory research flags for review by qualified U.S. regulatory counsel experienced in FDA dietary-supplement labeling (21 CFR Part 101). Reports reflect the documents provided and publicly available rules as of the report date. We do not test products, verify their contents, or guarantee compliance or any Amazon outcome. You remain responsible for compliance with applicable laws and marketplace policies.
To the maximum extent permitted by law, PanelCheckup's total liability for any claim arising from a report is limited to the amount paid for that report.
Start with one label at $99.
Name the service and attach what you already have. We’ll confirm whether the scope fits, identify anything missing, and give you a calendar due date after intake is complete. Capacity is capped at three active engagements; if full, we will offer a waitlist before accepting files.