FDA’s New Dietary Ingredient Notification — What It Means for You
The FDA has recently released new educational materials to help manufacturers and distributors navigate the new dietary ingredient notification (NDIN) review process. This process represents the agency’s only chance to evaluate the safety and identity of a new dietary ingredient before it reaches consumers. For supplement brands, especially those exploring innovative formulations, this update reinforces the importance of compliance from day one.
Having a well-organized, scientifically supported NDIN submission helps avoid costly delays or negative responses. The FDA’s latest fact sheet and videos outline common pitfalls in the notification process — including incomplete submissions or unclear ingredient identities — and provide guidance to streamline approvals. For brands, this means that working with a manufacturing partner who understands both compliance and production is not optional, but essential.
Consistency and reliability are also critical on the product side. Just as regulatory approval ensures safety, uniformity in production builds trust. To see how this applies to gummies, explore our article: Why Color Consistency Matters in Gummies.
What Beverage Manufacturing Can Teach Supplement Brands
While the FDA’s NDIN process applies to supplements, beverage brands can draw useful parallels. Entering the beverage market requires careful planning, attention to compliance, and strong partnerships with experienced manufacturers. Whether you’re launching a functional drink or a wellness-focused beverage, regulatory alignment ensures smoother market entry and fewer roadblocks along the way.
Private label and white label manufacturing models simplify the path to market. By leveraging the expertise of established facilities, brands gain faster turnaround times, access to compliance expertise, and the scalability needed to grow. For a clear breakdown of how these models work — and why aluminum cans remain the smartest choice — read Making Sense of White Label Beverage Manufacturing.
These lessons in agility and scalability apply equally to supplements. In a fast-moving industry, resilience and compliance aren’t just boxes to check — they’re part of your growth strategy.
Choosing the Right Format for Supplements
The FDA’s NDIN review emphasizes safety and identity — but your product format also plays a critical role in consumer trust. Whether liquid, powder, or liposomal, each delivery method comes with its own benefits, stability considerations, and regulatory expectations. Brands that align their choice of format with their market positioning will stand out while ensuring compliance with FDA expectations.
For example, liposomal supplements may offer enhanced bioavailability, while powders provide convenience and liquids cater to fast absorption. Understanding these trade-offs helps you select a format that meets both regulatory requirements and consumer preferences. To explore these options in depth, read Liquid vs. Powder vs. Liposomal Supplements — Which is Best?.
At Organic Supplement Manufacturing (OSM), we combine regulatory expertise with production excellence. From navigating NDIN requirements to ensuring your gummies, beverages, and supplements are consistent and compliant, we help you launch with confidence in today’s competitive marketplace.
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At Organic Supplement Manufacturing, our commitment to personalized service and clear communication sets us apart. If you’re looking for a partner who truly cares about your success, we’re here to help you create high-quality gummies that make an impact.
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