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Buyer questions · Purchase decisions

We are promoting a Retinol eye cream on Amazon US with the text 'clinically proven' and 'dramatically reduces wrinkles.' If complained about by professional complainers, can the factory provide efficacy substantiation files compliant with FTC standards and a response strategy?

The phrases 'clinically proven' and 'dramatically reduces wrinkles' constitute high-risk cosmetic claims requiring strong substantiation under FTC standards. The factory cannot provide substitute evidence. According to FDA regulations, proof must match the final product form, dosage, cycle, and target group. Complaints from professional complainers trigger platform penalties and civil claims, with factory liability limited to contract terms if its technical data is used.

1Evidence Matching & Risk Level

FTC requires human efficacy data matching the final product. In-vitro raw material data is insufficient. Delete high-risk text if evidence is missing to avoid false advertising claims.

2Factory Liability & Contractual Limits

Factories are not liable for terminal ads but are contractually bound if technical data is used. All external files must state 'not for terminal use' with sending records retained.

3Strategy for Professional Complainers

Prioritize removing high-risk text to stop losses. If no evidence exists, delete claims. Document client decisions; factories advise compliance but do not endorse claim legality.

Follow-up questions

Q:Can raw material data be used for US claims?
A:No. Evidence must target the final product form and dosage; in-vitro data does not support finished product claims.
Q:Does the factory bear fines for false claims?
A:Liability is limited to contractual reimbursement, not direct administrative penalties. Clients should document decisions in writing.

Figures sourced from:各国法规 · 美国美国护肤代工FDA 化妆品禁用与限用成分、色素添加剂配方库

Updated 2026-09-18

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