Healthcare professionals deserve clarity and confidence when it comes to the wellness guidance they share with their clients. This page is designed as both a trusted resource for understanding the complex regulatory landscape and a reflection of the Unilever Wellbeing Collective’s deep commitment to safety, compliance, transparency and scientific integrity. We invite you to explore how the Unilever Wellbeing Collective instills a culture of compliance grounded in safety, transparency, scientific integrity and regulatory excellence.
The foundation of every supplement begins with ingredients that must meet strict standards.
U.S. Food and Drug Administration (FDA) regulations require manufacturers, packers and holders of dietary supplements to follow Current Good Manufacturing Practices (cGMPs) to help ensure identity, purity, quality, strength and composition. The law prohibits the sale of adulterated products, and companies bear the responsibility to ensure their supplements are safe and compliant before they reach the market.
Our approach: Every Unilever Wellbeing brand uses carefully vetted ingredients, supported by internal quality assessments and safety reviews prior to market introduction.
Once ingredients are selected, the product must be manufactured under strict quality protocols. The FDA requires adherence to cGMPs for dietary supplements. These regulations govern everything from raw ingredient testing and process controls to documentation, sanitation and final product testing.
Current Good Manufacturing Practices ensure:
Ingredient identity and purity
Batch-level traceability
Consistent product quality
Unilever Wellbeing Collective brands follow all cGMP standards and brands like SmartyPants, Nutrafol and OLLY obtain third-party certifications for certain products, such as an NSF certification for added assurance.
What appears on a dietary supplement label — and in its advertising — is tightly controlled.
All dietary supplement product labels must indicate that it is ”Dietary Supplement” on the front of the label, along with the Net Quantity of Contents, or the amount of the product, a Supplement Facts Panel (SFP), Ingredient Statement and name and address of the manufacturer, packer or distributor, usually found on the side panel. Other common label elements include usage instructions or directions, warning statements and product claims. These claims must comply with FDA regulations and cannot suggest treatment or prevention of disease unless specifically approved.
Advertising claims are regulated by the Federal Trade Commission (FTC), which mandates that any health-related, structure/function or nutrient content claims be supported by competent and reliable scientific evidence. All advertising must be truthful, not misleading and substantiated prior to dissemination.
Every claim we make is reviewed for regulatory compliance and substantiation. We substantiate our products’ structure/function and health-related claims with high-quality science.
This information is provided as a medical and scientific educational resource for the use of dieticians and other licensed healthcare professionals. This information is intended for Practitioners to use as the basis for determining whether to recommend these products to their clients. All recommendations regarding protocols, dosing, prescribing and/or use instructions should be tailored to the individual needs of the client considering their medical history and concomitant therapies. This Information is not intended for use by consumers.