Turn ingredient lists and product information into compliant packaging artwork and print-ready files in 3–5 days, following Korean cosmetics law precisely. Use together with the packaging inspection agent to catch regulatory violations before launch.
Small cosmetics sellers and manufacturers need only provide an ingredient list and existing packaging. This agent analyzes current Korean Cosmetics Act, enforcement rules, and MFDS notices to compile all mandatory label content (product name, ingredients, warnings, expiration, business info, etc.), create layout mockups for your container type (carton, tube, bottle, label, pouch), and prepare print specifications for manufacturers. It flags risks like medical device classification or unsupported claims in advance.
What this agent produces
Core deliverables
- Packaging layout HTML mockup code (by container type)
- Copy spreadsheet (text, numerals, placement verification)
- Ingredient & allergen cross-reference table
- Usage warnings and precautions text
- Recycling symbol specs and material grading
- Online product disclosure statement (per E-commerce Act)
- Print file specs and production checklist (by container type)
When you need this
- Before launch: design primary/secondary packaging from scratch
- Existing packaging: missing or incorrect mandatory disclosures
- Functional claims (UV protection, whitening, etc.): translate approval documents into compliant label text
- Before printing: confirm file specs, font sizes, safety margins
- Formula or content changes: instantly identify which label items to update
How it works
Step 1: Collect product info (name, type, volume, ingredients, container specs)
Step 2: Verify packaging stage (primary/secondary) and functional product status
Step 3: Auto-generate label content per cosmetics law
Step 4: Flag incomplete data as {Confirm} and ask follow-up questions
Step 5: Self-check all output against 11 legal criteria (zero violations)
Step 6: Deliver print specs and vendor checklists
Important to know
- Legal citations included: Every requirement links to the specific law, enforcement rule, or MFDS notice.
- You handle procurement, filing, and approvals: This agent writes the content; you place print orders, apply for barcodes, and file functional product claims.
- Medical devices and unsupported claims are out: If your product looks like a drug or your claims lack evidence ("natural," "zero," etc.), the agent will refuse and explain why.
- Existing packaging revision: Upload a photo or PDF of current packaging and get a table of missing/wrong items plus fixes.
- Automated file analysis: Attach ingredient tables, packaging images, or functional approval documents—the agent reads and starts immediately.
