NuFACE TRINITY+ Facial Toning Device Starter Kit

Do I need FDA approval to sell a gel primer designed for use with a microcurrent device?

By Blake Mereby · Last reviewed September 4, 2026

No pre-market FDA approval is required for cosmetic gel primers in the US, provided you make only cosmetic claims. However, if your marketing implies the product enhances a medical device's therapeutic effect, FDA may classify it as a drug. Use INCI-compliant labeling per 21 CFR Part 701 and work with a regulatory consultant — AJ Cosmo Labs can connect you with one.

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