Getting it into your agent
One page per mod, every tool's command on it. A separate URL per tool would split the same page into five that compete with each other.
npx skills add Cleo-Labs-IA/skills_library --skill supplement-compliancegit clone --depth 1 https://github.com/Cleo-Labs-IA/skills_libraryWrote this? Show the measurements
A badge with what this costs and how it scanned, read live from this page, so it follows the numbers instead of freezing them. Markdown for a README, HTML for a documentation site or a project page.
[](https://agentmods.dev/skills/cleo-labs-ia/skills_library/supplement-compliance)<a href="https://agentmods.dev/skills/cleo-labs-ia/skills_library/supplement-compliance"><img src="https://agentmods.dev/badge/skills/cleo-labs-ia/skills_library/supplement-compliance/github.svg" alt="Measured on agentmods" height="20"></a>Or the 80×15 button, for a site that already has a row of RSS and ATOM ones. Only the verdict fits; the numbers stay here.
<a href="https://agentmods.dev/skills/cleo-labs-ia/skills_library/supplement-compliance"><img src="https://agentmods.dev/badge/skills/cleo-labs-ia/skills_library/supplement-compliance.svg" alt="Reviewed on agentmods" width="80" height="20"></a>What it costs to keep this loaded
Counted locally with the o200k_base tokenizer, which is exact for GPT models; Claude uses its own tokenizer and its counts differ. Treat this as one consistent yardstick across the catalogue rather than a bill. Prices are per million input tokens.
| Model | Per session | Once invoked |
|---|---|---|
| Fable 5.1 | $0.00065 | $0.03215 |
| Opus 5 | $0.00032 | $0.01607 |
| Sonnet 5 | $0.00013 | $0.00643 |
| Haiku 4.5 | $0.00006 | $0.00321 |
Grade A, and why
supplement-compliance scanned grade A with 0 findings against 26 rules in 11 categories — prompt injection, anti-refusal, data exfiltration, privilege escalation, supply chain, agent snooping, system-prompt leakage, SSRF and excessive agency — measured 12d ago.
A static scan of the body, not an audit. Every finding is printed with the line that produced it so you can judge whether it matters here. A mod is markdown that instructs an agent; that is exactly why what it instructs is worth reading.
Nothing flagged
None of the 26 patterns this scan looks for appear in this file: no shell pipes, no recursive deletes, no credential paths, no hidden text, no instruction-override or anti-refusal phrasing, no agent-config snooping. That is not a guarantee, it is the absence of the things that are checkable.
How it starts
The opening of the file, as written. The whole thing — 177 lines — stays where its author put it; the contents beside it link to each section on GitHub.
Supplement Compliance
Full regulatory workflow for dietary/food supplements, vitamins, minerals, botanicals, probiotics. Claims, GMP, country-specific registration.
Decision Flow
digraph {
rankdir=TB; node [shape=box style=rounded fontsize=10];
classify [label="1. Classify: supplement vs\nmedicinal vs novel food vs cosmetic"];
ingredients [label="2. Ingredient screen\n(positive lists, novel food status)"];
claims [label="3. Claims review:\nstructure/function vs disease"];
gmp [label="4. GMP compliance\n(21 CFR 111 / GMP+ / KGMP)"];
reg [label="5. Country registration\n(notification or pre-approval)"];
label [label="6. Market-specific labels"];
rp [label="7. Local representative\n(EU FBO, China holder, Korea agent)"];
sell [label="8. Place on market"];
classify -> ingredients -> claims -> gmp -> reg -> label -> rp -> sell;
}
US -- FDA DSHEA
| Requirement | Detail |
|---|---|
| Legal basis | Dietary Supplement Health and Education Act 1994 (DSHEA), FD&C Act 201(ff) |
| Definition | Product containing vitamins, minerals, herbs, amino acids, or dietary substances. Cannot be marketed for disease treatment |
| Pre-market | NO pre-market approval. BUT New Dietary Ingredient (NDI) notification required for ingredients NOT marketed pre-Oct 15, 1994. Submit 75 days before marketing |
| Facility registration | Required under FSMA. Renew biennially (even years Oct 1-Dec 31) |
| GMP | 21 CFR Part 111 -- mandatory for all manufacturers, packers, holders, labelers. Includes identity testing of each incoming dietary ingredient |
| Labeling | "Supplement Facts" panel (not Nutrition Facts), structure/function disclaimer "These statements have not been evaluated by the FDA. This product is not intended to diagnose, treat, cure, or prevent any disease." -- mandatory if claim made |
| Claims | Structure/function permitted (e.g., "supports immune function"). Disease claims PROHIBITED (e.g., "cures cancer"). Submit notification to FDA within 30 days of first use |
| Adverse event reporting | Serious AEs reportable to FDA within 15 business days (DSHEA section 761) |
| Cost | Facility registration: $0. NDI notification: $0 (but $20,000-100,000 in toxicology data). 21 CFR 111 GMP audit: $5,000-25,000 |
What this file has done since we first saw it
Hashed on every crawl. A supply-chain change to an agent config is a question of when, not whether, so the history is kept rather than the latest state alone.
- 12d ago First seen · 177 lines · 65 tokens per session scan A 8df0d7fdcec7
supplement-compliance is a skill published in the GitHub repository Cleo-Labs-IA/skills_library (1 stars, last pushed 3mo ago), licensed MIT. It adds 65 tokens to every session and 3,215 once invoked, about $0.0003 per session on Opus 5. A static security scan graded it A with 0 findings. No closer match exists in the catalogue, so it is treated as the original; first seen 2026-08-31.
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