FDA product listing, facility registration, and the responsible person.
How to work through the MoCRA small business exemption for facility registration and product listing, and which obligations it does not waive.
Clearing up whether the brand owner, contract manufacturer, or distributor is the MoCRA responsible person, with examples for each setup.
A worked walkthrough of assembling MoCRA safety substantiation for a small-batch product line, from existing ingredient data through toxicologist review.
What the MoCRA small business exemption actually covers for micro-sellers, and the common assumptions about hobby scale that don't hold up.
Canceling a listing under MoCRA doesn't end your obligations. Here's what records and reporting duties stay open.
Which cosmetic categories never qualify for the MoCRA small business exemption, no matter how small your revenue is.
MoCRA expanded FDA's records access and inspection reach for cosmetic facilities, and small operations should know what a visit involves.
MoCRA mandates a formal cosmetic GMP rule from FDA. It isn't final yet, but small makers who start now won't be scrambling later.
What can trigger an FDA-ordered cosmetic recall under MoCRA, and how a responsible person should react if it happens.
What the second tranche of Canada's fragrance allergen disclosure requires and how it builds on the List 1 deadline from earlier in 2026.
The US-specific steps a Canadian soap and cosmetic maker needs on top of their existing CNF work, from facility listing to the drug-cosmetic line.
How salon and spa professional-use products are treated under MoCRA, including the professional-use labeling statement.
A practical walkthrough of creating your FDA account for cosmetic facility registration and product listing under MoCRA.
MoCRA leaves true soap outside FDA cosmetic rules, but a soap makes a cosmetic claim and falls inside MoCRA the moment it promises to moisturize or clear skin.