Sell Your Cosmetic Products in the USA
Choose the right MoCRA support for your cosmetic facility and products. We check whether registration or listing applies before preparing the agreed work.
Individual Services
If you only need one filing or one review, you can order that service without taking a full bundle.
FEI Number Acquisition
One-time
$149
Cosmetic Facility Registration
This filing-only offer requires an existing FEI and, for a foreign facility, an appointed U.S. agent. If either record is missing or uncertain, ask us to check the right scope before payment.
$349
Cosmetic Product Listing
Professional fee per product; eligible variants may share an FDA listing
$75 per product
Cosmetics Label Review
Per unit
$249 per label
Cosmetic Product Listing + Label Review Bundle
Per unit
$249 per product
FDA Cosmetic Facility Renew + US Agent Transfer
Recurring
$349
Cosmetics bundles
Choose the bundle that matches your stage: a first facility registration or a wider launch with product listings and label reviews included.
Cosmetics Starter
$449
- FEI Number Acquisition
- Cosmetic Facility Registration
- US Agent (Year 1 included)
Cosmetics Brand Launch
$1,249
- FEI Number Acquisition
- Cosmetic Facility Registration
- US Agent (Year 1 included)
- 5 product listing service units (FDA filing groups may differ)
- 5 Label Reviews
Year 1 is 12 months from acceptance of FDABridge’s U.S. Agent designation in the FDA record. No automatic renewal; continued coverage needs a separate written scope, quote and payment before the period ends.
Unless separately agreed in writing, Agent coverage excludes DUNS/FEI, filings and renewals, amendments, listings, label review, Prior Notice, FSVP/importer, laboratory, customs/broker, legal, inspection response and Import Alert/detention work.
Completion evidence is the applicable FDA record and accepted Agent designation. DUNS/FEI evidence comes only with bundles that include it. This is not FDA approval or guaranteed import clearance.
What MoCRA means for cosmetic brands
Use this short overview to compare responsibilities and decide which service fits your facility and products.
FD&C Act section 607, added by MoCRA, separates facility registration by a covered facility's owner or operator from product listing by the manufacturer, packer or distributor named on the cosmetic label.
Check the actual activity and product: certain small businesses and certain drug or device products or facilities may be exempt. The small-business exception does not cover specified products that regularly contact the eye mucous membrane, are injected, are intended for internal use, or alter appearance for more than 24 hours without customary consumer removal.
FDA uses FEI as the cosmetic facility registration number; DUNS is optional here. An exempt facility without a required registration number may be identified by name and address in a product listing.
A newly covered facility generally registers within 60 days of first manufacturing or processing cosmetics for U.S. distribution, subject to the statutory transition dates. A required facility registration renews every two years from its own initial date, with applicable registration changes generally amended within 60 days. New product listings are generally due within 120 days of first marketing, with annual updates; some qualifying variants may share a listing.
Questions cosmetic brands ask before selling in the US
These are the common questions we hear from foreign manufacturers and brand owners before they start their MoCRA-related filings.
What is MoCRA in simple terms?+
MoCRA added FD&C Act section 607 facility registration and product listing, with distinct owners and exemptions. FDA does not approve or certify cosmetic products through these submissions.
Do foreign cosmetic brands need to register before selling in the USA?+
A foreign cosmetic manufacturing or processing facility may need registration if its activity and products are covered and no exemption applies. The label-named responsible person handles a separate product listing. Check the actual scope before filing or ordering a service.
What is an FEI number?+
FDA uses its Establishment Identifier (FEI) as the cosmetic facility registration number. Check for an existing FEI before requesting one. DUNS is optional information for this filing, not a substitute for FEI.
Do I need to list every cosmetic product?+
A covered marketed product must be listed by its label-named responsible person, but FDA permits one listing for identical formulations or variants differing only in color, fragrance, flavor or quantity. Our per-product professional fee is a separate billing unit.
Why is label review important for cosmetics?+
A label review helps catch issues before they create problems in the market. It is a practical way to reduce avoidable mistakes in product presentation and claims.
Do I need a US Agent for cosmetic facility registration?+
A foreign facility that must register supplies its appointed U.S. agent information and FEI. The $349 facility service covers the filing only; FEI acquisition and first-year agent coverage are separate. The $449 Starter adds FEI acquisition and retains its stated first-year agent coverage. The agent is not automatically the label-named responsible person or an importer.
How long does the cosmetics registration process take?+
Preparation depends on complete details, existing FEI status, classification and scope. FDA processing is separate, and a submission or number is not approval, certification or an admission guarantee.
What happens after I place an order?+
You submit the application for the selected professional service. We check scope and prepare agreed work, then share the available submission and status record. Request acknowledgement, payment, FDA processing and regulatory completion are distinct.
Related Blog Articles
MoCRA Cosmetic Facility Registration: Who Registers and What Changed
Apr 7, 2026
A practical guide to facility owner/operator registration, the label-named responsible person, FEI, exemptions, renewal and product listing under FD&C Act section 607.
Cosmetic Product Listing Under MoCRA: Responsible Person, Grouping and Updates
Jul 10, 2026
Who lists cosmetics with FDA, what Form 5067 requires, when certain variants may share a listing, and how initial and annual updates work.
MoCRA basics for cosmetic brands outside the United States
Mar 7, 2026
A simple starting guide for foreign brands preparing facility registration and product listing under the newer cosmetics rules.