Instantly check 4012+ ingredients against FDA MoCRA, EU SCCS, Japan MHLW, and Korea MFDS regulations. Know what's prohibited, restricted, or requires drug approval — before you sell cosmetics or pharmaceuticals in any market.
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No forms. No waiting. Paste your ingredient list and get an instant verdict.
Copy your formula's ingredient list — comma-separated, one per line, or raw text. Our parser handles messy exports from any lab or supplier.
Every ingredient is matched against FDA MoCRA database. See status, concentration limits, and required actions in under a second.
Download a PDF compliance report for your records or regulators. Upgrade for bulk Excel/PDF uploads and unlimited checks.
Built for cosmetic and pharmaceutical manufacturers, formulators, and regulatory consultants selling in the U.S..
See US, EU, Japan, and Korea regulatory status side-by-side. Know if your ingredient is a cosmetic in one market but a drug in another.
Paste 50+ ingredients at once. Fuzzy matching catches spelling variations and common aliases.
Paid subscribers can isolate cosmetics from pharmaceuticals. Formulators don't need drug monograph noise; regulatory consultants need focused reports.
Generate branded PDF compliance reports with your logo for regulators, clients, or internal QA.
Database synced with FDA changes. Never get caught off-guard by a new ban or restriction.
Every result includes exact 21 CFR sections, actual FDA Warning Letter references, and combination restrictions. ChatGPT hallucinates CFR numbers. We don't.
Get warned when an ingredient crosses from cosmetic to OTC drug or quasi-drug status by jurisdiction. Avoid regulatory misclassification.
Regulatory consultants charge $300–500/hour. A misclassified ingredient can create compliance risk, product delays, and legal costs. Our Starter tier helps you spot issues early — before they become expensive problems. This tool is for informational purposes; always verify with a qualified regulatory professional.
Ch*tGPT hallucinates CFR sections. We provide real 21 CFR 700.11, 21 CFR 352.10, 21 CFR 333.301 citations. When FDA audits your files, you need the exact subsection — not a confident guess.
Ch*tGPT cannot reliably tell you the exact % where an ingredient flips from cosmetic to OTC drug. We do: Hydroquinone 2% = OTC drug vs cosmetic. Salicylic Acid 0.5–2% = OTC for acne. Miss the threshold, miss the market.
Ch*tGPT gets Japan/Korea/US/EU comparisons wrong constantly. Minoxidil: OTC drug in US, functional cosmetic in Korea, quasi-drug in Japan, medicinal product in EU. This is non-obvious. One wrong assumption = detained shipment.
We explain the intent-based classification: same ingredient, same concentration, but different claims = different regulatory path. This is lawyer-level nuance that LLMs struggle with. FDA does not care what the LLM "thinks."
Ch*tGPT answers in prose. Our structured database enables: batch checking 50+ ingredients, PDF export with exact citations, fuzzy matching across 1,000+ synonyms, filtering by restriction type / category / jurisdiction. Speed matters when a client is waiting.
Research backed by Semantic Scholar API — Burdock 2024 on MoCRA, Yoshitomi 2025 on JSQDI, Kojima 2021 on quasi-drug testing. When your legal team asks "where did this data come from," you have a real citation. Not a hallucinated "source."
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