# Check my dietary supplement labels and marketing for FDA compliance risks

Flags disease claims, missing disclaimers, and labeling gaps in supplement packaging and ads under US FDA and FTC rules.

- Topic: Legal & Compliance
- Framework: RTF
- Level: Standard
- Tags: Legal, Marketing, Health & Wellness, Analyze, Code, Fill-in Template
- Source: https://www.thinkwithprompt.com/prompts/check-my-dietary-supplement-labels-and-marketing-for-fda-compliance

## Prompt

```text
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.
```

## What to fill in

- NAME, form, ingredient list with amounts
- PASTE front panel, Supplement Facts, directions, warnings
- any ingredient not marketed in the US before 1994, if known
- in-house / contract manufacturer

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