Check my dietary supplement labels and marketing for FDA compliance risks

Review my dietary supplement's label and marketing for US regulatory risk. Product and ingredients: [NAME, form, ingredient list with amounts] Label text: [PASTE front panel, Supplement Facts, directions, warnings] Marketing copy: [PASTE website, Amazon listing, ads, social posts, testimonials] New ingredients? [any ingredient not marketed in the US before 1994, if known] Manufacturing: [in-house / contract manufacturer] Check against these areas (DSHEA framework, FDA labeling rules, FTC advertising rules): 1. Claims - sort every claim into: structure/function (allowed with disclaimer), authorized health claim or qualified health claim, nutrient content claim, or implied disease claim (treat, cure, prevent, mitigate a disease - not allowed). Pay attention to implied claims through images, testimonials, product names, and hashtags. 2. Required disclaimer - the FDA "has not evaluated" statement wherever structure/function claims appear, and the 30-day notification to FDA. 3. Label elements - statement of identity including "dietary supplement", net quantity, Supplement Facts panel format, ingredient list, manufacturer/distributor info, allergen labeling. 4. Advertising substantiation - whether each claim likely needs competent and reliable scientific evidence, and claims that look unsupported; testimonial and endorsement disclosures. 5. Other flags - possible new dietary ingredient notification, ingredients FDA has warned about, cGMP responsibilities for the brand owner. Return a table: Claim or element | Location | Issue | Risk (high/med/low) | Suggested compliant rewrite. Then a short list of questions for my regulatory counsel. This is general information, not legal advice. Rules change; have a qualified regulatory attorney or consultant confirm before printing labels or launching.