Everything you need to sell cosmetics in the U.S. — facility registration, product listing, U.S. Agent service, and label review. Handled by our Miami-based team.
Many facilities that manufacture or process cosmetic products for distribution in the U.S. may be required to register with FDA under MoCRA, subject to applicable exemptions. Our team prepares and submits your facility registration, helps you obtain an FEI number if needed, and helps you stay on top of the biennial renewal cycle.
The responsible person must list each marketed cosmetic product with FDA, including product ingredients and other required listing information, and provide annual updates. Our team compiles your Structured Product Labeling (SPL) data and submits the product listing on your behalf.
Important: Cosmetic product listings must be updated annually and whenever material product information changes, while facility registration must be renewed every 2 years. These timelines are separate, and we help you manage both.
Foreign cosmetic facilities that are required to register must designate a U.S. Agent located in the United States and authorized to receive FDA communications on their behalf. Our Miami office serves as your registered U.S. Agent and forwards FDA correspondence to you promptly in English or Spanish.
U.S. cosmetic labels may need to include required elements such as ingredient declaration, net contents, responsible party information, category-specific warnings, and country-of-origin information when applicable. Our team reviews your front and back labels against MoCRA and FDA cosmetic labeling guidance before your product reaches the U.S. market.
Send us your label artwork and we’ll provide a detailed quote along with initial observations. Standard review turnaround: 10 business days from approval.
Choose the plan that fits your business.
Not sure which plan? Schedule a free 20-min call →
Complex cases, multi-facility setups, or non-standard scenarios? Tell us about your business and we’ll build a scope just for you.
