AEG expertise / Dietary Supplements
Nutrition analysis, labeling, and regulatory support for dietary supplements. Aimee brings experience developing supplement panels, evaluating product claims, and reviewing label artwork within the sports nutrition industry.
Discuss your productU.S. FDA-regulated dietary supplements. Review covers 21 CFR Part 101, including § 101.36; ingredient and allergen requirements; and the DSHEA structure/function framework, including disease-claim risk and questions about disclaimers and notifications.
The proposal identifies deliverables, file formats, estimated hours, and artwork review stages. Work is billed hourly, including revisions; the project estimate sets out the agreed scope.
Genesis R&D-based panel work averages about one week from a complete formula and supporting documents. Claims-only review, artwork-only review and on-shelf label audits receive a project-specific delivery date after Aimee assesses the scope and materials.
Laboratory testing, legal opinions, USDA labeling or approval, Canadian labeling, Proposition 65 assessments, NDI notifications, claim-substantiation dossiers, and regulatory filings are outside the standard label-review scope.
Any notification, new dietary ingredient, or substantiation issue is flagged. Additional work or specialist involvement must be assessed and agreed separately; it is not included or promised by a panel review.
A closer look
Develop and review Supplement Facts information with attention to serving size, dietary ingredients, quantitative amounts, % Daily Value where required, and the underlying formula and raw-material data. Aimee’s background includes constructing supplement panels using Genesis R&D.
Coordinate dietary and other ingredients, allergen information, flavors, colors, excipients, and source ingredients with raw-material specifications and the documentation needed to support the label.
Evaluate structure/function language and other proposed product messaging for scientific accuracy, substantiation, and disease-claim risk, drawing on experience working with Scientific Affairs and Legal teams.
Review preliminary and final label artwork against the agreed panel and claim set, with experience coordinating label specifications, cross-functional approvals, and supporting documentation before launch.
Describe the supplement format and claims you want reviewed. Aimee confirms the workstreams, required evidence and schedule before work begins.
Send a project brief ↗Across categories
Illustrative example—not an actual client case.
Draft label wording
“Prevents colds and flu.”Remove or revise
This wording claims to prevent disease. It is not a dietary supplement structure/function claim, and a disclaimer does not resolve the disease claim.
Remove the wording. Assess whether evidence supports a statement about normal immune function for the actual ingredient, dose, product, and population before considering replacement language.
Reference: FDA structure/function claims guidance.
Start with the label
Tell her the product, market, print date, and decision: new panel, reformulation, claim, or artwork check.
For a supplement review, describe the format, proposed claims and intended launch date.
Registered dietitian · Founder
AEG Consulting LLC · Greater Chicago Area