Navigating FDA Compliance for Supplement Labels
How does a contract manufacturer HELP ensure my product label is FDA compliant?
You’ve poured time, passion, and capital into perfecting your unique supplement formula. The next crucial step is designing the label—the vital communication tool that connects your product with your customer. This label needs to do two things perfectly: capture attention and adhere to the law.
The world of FDA regulations for dietary supplements is intricate, governed by the Dietary Supplement Health and Education Act (DSHEA). It’s about precision: ensuring every claim, ingredient list, and disclaimer is correct. This isn’t just about meeting a requirement; it’s about establishing immediate trust and long-term brand credibility.
This is where choosing a knowledgeable, full-service contract manufacturer becomes your greatest strategic advantage. A trusted partner ensures FDA compliance by managing the entire labeling process from concept to carton. This includes reviewing claims (differentiating legal structure/function claims from impermissible disease claims), recommended formatting of your Supplement Facts panel, and the accurate placement of all required warnings and disclaimers.
Our In-House Design & Compliance Advantage
At Quality Supplement Manufacturing, we offer more than just manufacturing; we offer peace of mind. Our integrated labeling service combines expert compliance with seamless design support. By handling both the manufacturing and the complex label design/review process in-house, we eliminate the need for you to coordinate between multiple regulatory consultants and graphic designers. We manage the detailed, nuanced work, ensuring the label we print is the same label we approved.
Our expertise helps you navigate the regulatory landscape with confidence, ensuring your product is market-ready without delays or complications.
Ready to launch your product knowing your labeling is built for success and compliance?
