Prepare a supplement, cosmetic, food or device label for U.S. review

What to prepare

What the result means

1. Enter exact product facts or label text, then review the detected fields before confirming them.
2. Confirmed facts run published rules against the current product version. Missing evidence remains visible.
3. Automatic OCR has not yet met the full-label reliability target and is not available in this public pilot.
4. The result is a preliminary screen, not FDA approval or legal advice.

How to get a useful first check

Keep every panel of the current artwork available, including folds, narrow side panels, cap or lid text, and inserts. Enter facts or paste exact readable text for this preliminary check. Automatic image uploads are currently disabled because full-label reliability has not been demonstrated. Do not reconstruct unreadable text or assume that a missing field is absent from the product.

For supplements and foods, enter the formula and serving basis when relevant. For cosmetics, use the ingredient list and intended use. For devices, use the exact model, intended use, instructions, warnings and known materials rather than a food-style ingredient list. Record the business role and exact claims for every category. Do not substitute a supplier sheet for finished artwork or reuse facts from a similar SKU. Confirming supplied facts does not establish extraction accuracy, market authorization or complete legal compliance.

Use the findings as a review queue

Start with blocked rule execution, missing evidence, and claim or ingredient findings marked critical or high. Open the cited source, confirm whether it applies to the product, and record the corrected fact or artwork version. Re-run the assessment after a material change rather than treating an older result as current.

• FDA Dietary Supplement Labeling Guide
• FDA Food Labeling Guide
• 21 CFR Part 101 — Food labeling
• FDA Cosmetics Labeling Guide
• 21 CFR Part 701 — Cosmetic labeling
• FDA Device Labeling