FIXED PRICE, FIXED SCOPE

Label review and product registration, done for you.

Q: Does MoCRA listing make my product FDA approved?

No. The FDA does not approve cosmetics. Listing is a requirement, not an endorsement.

Q: Who is the Responsible Person for the EU and UK?

A partner company established in that market, quoted separately and shown before you pay.

The paperwork between a finished formula and a legal sale. Fixed prices, fixed scope, handled by the team that already keeps an FDA-registered facility in order.

PayChoose the market, pay online
UploadLabel artwork, formula, supplier documents
We fileReview, correct, submit
ConfirmedListing numbers and marked-up files back to you

FDA-registered facilityMoCRA, CPNP and SCPNWritten scopeNo retainer

Stainless clipboard, pipette and a frosted jar on a lab bench

PRICES

Start with the label. Add the markets you sell in.

Every service starts with the label, because that is where most problems are. US Ready adds the FDA listing. Global Ready adds the EU and UK notifications in the same order, with the saving shown.

US label and claims review

Before you print.

USD 350per product

Ingredient declaration checked against INCI and 21 CFR 701
Claims checked for drug language and unsupported statements
Warnings, net quantity, responsible person line and font sizes
Marked-up PDF plus a corrected text block you can paste to your designer
One re-check of the revised artwork

Most chosen

US Ready

Label review plus the FDA MoCRA listing, in one order.

~~USD 800~~Save USD 100

USD 700per product

Everything in the label and claims review
FDA MoCRA cosmetic product listing in Cosmetics Direct
Facility registration link to the manufacturing site
Adverse-event contact line and record template
Listing confirmation sent to you with the FDA listing number

Global Ready

US, EU and UK in one go.

~~USD 2,300~~Save USD 350

USD 1,950per product

Everything in US Ready
EU CPNP notification with a partner Responsible Person
UK SCPN notification with a partner Responsible Person
Product Information File gap check (what you have, what is missing, who supplies it)
One label set adapted for EU and UK wording

Responsible Person retainer fees from the partner are quoted separately and paid to the partner.

Fixed scope, no surprises. Scope is fixed before we start. If we cannot deliver the scope you paid for, you get the unused part back. No subscription, no retainer.

SINGLE SERVICES

EU CPNP notification

USD 900per product

With a partner Responsible Person; PIF gap check included.

UK SCPN notification

USD 700per product

With a partner Responsible Person; PIF gap check included.

FDA MoCRA listing only

USD 450per product

Product listing and facility link, no label review.

WHAT YOU GET

Documents you can hand to a retailer

Marked-up label PDFEvery change explained with the rule it comes from, plus a clean text block for your designer.

Listing confirmationsThe FDA listing number, the CPNP or SCPN reference, and a one-page summary of what was filed and when.

PIF gap listWhat your Product Information File has, what it is missing and who supplies each piece (us, your packaging supplier, the test lab).

Records templateAdverse-event log and change log, so the listing stays valid after launch.

HOW IT WORKS

Four steps, most of them ours

STEP 01

Upload

After payment: label artwork, formula or INCI list, and any supplier documents you already have.

DAY 0

STEP 02

Review

We check the label and the file against the rules for each market and send the marked-up version.

WITHIN 5 BUSINESS DAYS

STEP 03

Submit

Once the label is right, we file the listing or notification. EU and UK filings go through the partner Responsible Person.

WEEK 2

STEP 04

Confirm

Reference numbers, the filed documents and the records template arrive in one email.

ON CONFIRMATION

Government and Responsible Person fees, where they apply, are not included and are shown before you pay. Timelines depend on the authority's processing; we report progress weekly.

ADD-ONS

Chosen at checkout

Additional product in the same order

40% off

Same brand, same service, 40% off the second product onward.

Safety data sheet (SDS) for the finished product

USD 250

GHS format, for shipping and retail onboarding.

60-minute compliance walkthrough

USD 200

Screen share: how to keep your listing, adverse-event records and PIF current.

QUESTIONS

Before you buy

Is this legal advice?

No. It is regulatory preparation and filing by a cosmetics manufacturer that keeps its own registrations current. For a legal opinion on a claim, we tell you when you need a lawyer rather than guess.

Does MoCRA listing make my product "FDA approved"?

No. The FDA does not approve cosmetics. Listing is a legal requirement for most cosmetic products sold in the US; it is not an endorsement, and we will not let a label say otherwise.

Who is the Responsible Person for the EU and UK?

A partner company established in that market. Their retainer is quoted separately, paid to them, and shown to you before you pay us.

What if my product is not made by GFE?

That is fine. The label review and the listings work for products made anywhere, as long as you can supply the formula and the manufacturer's details.

STILL DEVELOPING THE PRODUCT

Buy the formula and the compliance together

Launch Formula includes the US listing and the label review, with a production slot held for you.

See formulation prices Book a 30-minute call