United States · Cosmetics

Cosmetic Good Manufacturing Practice in the United States

A practical guide to Cosmetic Good Manufacturing Practice for cosmetics sold in the United States: who it applies to, what to prepare, and the mistakes that cause rejection.

Who needs it
Brands and importers placing cosmetics on the market in the United States; Online sellers listing cosmetics for buyers in the United States
Authority
U.S. Food and Drug Administration
Legal basis
21 CFR Part 702
Local representative
A local responsible entity or authorised representative is required
Timeline
Before sale; notification review typically takes weeks
Cost
Official fees are usually low; testing and local representation add cost
If you do not comply
Recall, import block, fines, or marketplace delisting

Who needs this

Documents you need

Compliance checklist

Tick each item as you collect it. Saved in this browser only.

How to comply

  1. Confirm the product is legally a cosmetic in this market
  2. Compile the product information file and safety assessment
  3. Complete the local notification or registration step
  4. Check labels, warnings, and claims against local rules

Brief for your lab or agent

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Request: Cosmetic Good Manufacturing Practice — United States
Product category: Cosmetics
Authority: U.S. Food and Drug Administration
Legal basis: 21 CFR Part 702

Documents we already have:
  1. Product information file with a safety assessment
  2. GMP certificate for the manufacturing site
  3. Ingredient and labelling compliance review
  4. Local notification, registration, or acknowledgement

Questions:
  1. Does our product fall under Cosmetic Good Manufacturing Practice in the United States?
  2. Which test standards or evidence do you accept?
  3. What is the current fee and lead time?
  4. Is a local representative required, and can you act as one?

Cost and timeline

Before sale; notification review typically takes weeks.

Official fees are usually low; testing and local representation add cost.

Common rejection reasons

Registration, notification, or certification is not the same as approval. Keep the technical file current and make sure the label, listing, and submitted data match.

Official sources

FAQ

Who needs Cosmetic Good Manufacturing Practice in the United States?

Brands and importers placing cosmetics on the market in the United States. Online sellers listing cosmetics for buyers in the United States. The importer of record normally holds the evidence.

What documents do I need for Cosmetic Good Manufacturing Practice?

Product information file with a safety assessment; GMP certificate for the manufacturing site; Ingredient and labelling compliance review; and local notification, registration, or acknowledgement.

What is the first step for Cosmetic Good Manufacturing Practice?

Confirm the product is legally a cosmetic in this market, then compile the product information file and safety assessment. Before sale; notification review typically takes weeks.

How long does Cosmetic Good Manufacturing Practice take?

Before sale; notification review typically takes weeks.

How much does Cosmetic Good Manufacturing Practice cost?

Official fees are usually low; testing and local representation add cost.

What happens if I sell without it?

Recall, import block, fines, or marketplace delisting.

Who regulates Cosmetic Good Manufacturing Practice in the United States?

U.S. Food and Drug Administration.

Related requirements

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