The registration details, in plain text
Retailers, insurers, contract auditors and Amazon category reviewers all ask for the same three data points. Here they are, so you can paste them straight into a vendor form.
- Legal entity: TV Manufacturing, LLC — DBA SkinCore Labs
- FDA Establishment Identifier (FEI): 3048933157
- MoCRA cosmetic facility registration: Submission Accepted
- Facility: 2320 E Locust Ct, Unit C2, Ontario, CA 91761, USA
What MoCRA actually requires of a manufacturer
The Modernization of Cosmetics Regulation Act gave the FDA real authority over cosmetics for the first time since 1938. For a contract manufacturer, three obligations matter most: facility registration renewed biennially, product listings filed for every cosmetic product manufactured, and adverse event records retained and reportable.
MoCRA also adds mandatory safety substantiation, fragrance allergen disclosure on labels, and FDA power to order mandatory recalls. None of that is optional, and none of it can be retrofitted after a launch goes wrong.
- Biennial facility registration with the FDA
- Product listing for each cosmetic product manufactured
- Safety substantiation records for every marketed formula
- Adverse event recordkeeping and serious-event reporting within 15 business days
- Good Manufacturing Practice conformance as FDA finalizes the rule
Why the responsible person still carries obligations
A registered manufacturer does not absolve the brand. Under MoCRA the 'responsible person' — usually the brand whose name is on the label — owns the product listing, the safety substantiation file and the adverse event reporting duty.
We supply the manufacturing side of that file: batch records, specifications, stability data, micro testing and the facility registration number your listing references. You keep the responsible-person obligations. We tell founders this early because discovering it during a retailer audit is expensive.
What this changes in a real project
Practically, working with a registered facility shortens diligence. Retail buyers at Ulta, Sephora, Target and Credo ask for the FEI before a purchase order. Insurers ask for it before binding product liability. Amazon asks for it during cosmetic category ungating. Having the number, the accepted MoCRA submission and the supporting documentation on file removes weeks from those conversations.
It also matters for private-label and government contract work, where facility registration is a hard gate rather than a preference.
Key takeaways
- SkinCore Labs operates under TV Manufacturing, LLC with FDA Establishment Identifier 3048933157.
- Our MoCRA cosmetic facility registration submission has been accepted.
- MoCRA obligations split between the facility (registration, GMP, records) and the responsible person (listing, safety substantiation, adverse events).
- A registered facility shortens retailer, insurer and marketplace diligence from weeks to days.