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I will do fda mocra cosmetic facility registration and product listing
Helen G
About this gig
Are you a cosmetics brand selling in the US? In 2026, the FDA is actively enforcing MoCRA mandates, conducting audits, and requiring the first wave of biennial facility renewals. Non-compliance risks warning letters, custom detentions, or forced market recalls.
As an expert regulatory compliance consultant, I will handle the technical complexities of the FDA Cosmetics Direct portal, ensuring your business stays fully compliant.
What I Can Do For You:
- FDA FEI Number Acquisition & Verification
- FDA Facility Registration (Form 5066) 2026 Biennial Renewals
- Cosmetic Product Listings (Form 5067) including complete ingredient structuring
- Mandatory Labeling Reviews (including adverse event contact pathways)
- Product Safety Substantiation File Organization & Templates
- Serious Adverse Event Reporting SOP Templates (Mandatory 15-day FDA reporting compliance)
Please Note: For international brands, I provide full documentation, portal data compilation, and submission prep. However, you must provide your own domestic U.S. Agent address for the final submission, as required by the FDA.
Message me today with your product count, and let's secure your spot in the US beauty market!
Get to know Helen G
Helen G
Regulatory Compliance Specialist, Professional Archival Researcher
- FromUnited States
- Member sinceMar 2026
- Avg. response time1 hour
Languages
English, French
Professional Researcher and Compliance Specialist offering expert assistance in U.S. FDA regulatory requirements and archival genealogy research.
FDA & MoCRA Services:
• Food & Supplement Label Audits
• MoCRA Cosmetic Facility Registrations
• Product Listings & Import Compliance
Genealogy & Ancestry Services:
• Jewish Ancestry & Immigration Records
• Family Tree Building & Archival Document Search
With deep attention to detail, I deliver fast, fully compliant, and accurate research solutions tailored to your unique needs. Message me to discuss your project
FAQ
What do you need to start my product listing?
I need your ingredient lists (INCI names), product names, packaging labels, your business address, and your facility’s FDA Establishment Identifier (FEI).
Can you act as our physical U.S. Agent?
No, I do not provide a U.S. physical address. I will prepare all of your submission data, but you must provide your own U.S. resident agent to finalize the filing.
What is a Serious Adverse Event SOP?
It is a mandatory written procedure showing how your brand logs and reports severe health reactions to the FDA within 15 business days. I provide the exact template you need.
Do small cosmetic brands needs safety substantiation?
Yes! While brands under $1M in sales have some exemptions, all brands must maintain scientifically backed safety records for every product to prevent FDA recalls.
Can you help if I don't have an FEI number yet?
Absolutely. I will search the FDA database to see if one exists or help you submit a request to the FDA to generate a new FEI number for your facility
