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FD&C Act §607 (MoCRA)

FDA U.S. Agent for cosmetic facilitys in Thailand

A cosmetic facility in Thailand that exports to the United States must register with FDA and name a U.S. Agent located in the U.S. (FD&C Act §607 (MoCRA)). In the 12 months from 2025-10 to 2026-09, FDA refused 418 import lines from Thailand, and 50 FDA import alerts list firms from Thailand.

FDA data for Thailand

Figures from FDA public data, retrieved 2026-10-21. Recall counts are by the recalling firm's country.

Import refusals, 2025-10 to 2026-09

Refused import lines418
Refusals citing registration or listing problems
NOT LISTED-118 · 39

Most common refusal charges

CodeCount
FILTHY-249
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise un…
106
UNAPPROVED-75
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
56
PESTICIDE-241
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the …
42
NOT LISTED-118
The article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. Based on the information…
39
SALMONELLA-9
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.
38

Import alerts listing Thailand firms

Import alerts that list at least one firm in Thailand: 50. Recently updated:

  • Import Alert 16-129: Detention Without Physical Examination of Seafood Products Due to Nitrofurans
  • Import Alert 16-39: Detention Without Physical Examination of Ready-to-Eat Seafood for Listeria monocytogenes
  • Import Alert 20-07: Detention Without Physical Examination of Juice from Foreign Processors Not in Compliance with Juice HACCP Regulation
  • Import Alert 45-02: Detention Without Physical Examination and Guidance of Foods Containing Illegal and/or Undeclared Colors.
  • Import Alert 99-05: Detention Without Physical Examination Of Raw Agricultural Products for Pesticides
  • Import Alert 99-08: Detention without Physical Examination of Processed Human and Animal Foods for Pesticides

What the rule requires

Under the Modernization of Cosmetics Regulation Act (MoCRA), foreign facilities that manufacture or process cosmetic products for U.S. distribution must register with FDA and include the name and contact details of a U.S. Agent. Registrations are renewed every two years, and product listings are updated every year.

  • Foreign facilities that manufacture or process cosmetic products distributed in the U.S.
  • Small businesses as defined in FD&C Act §612 may be exempt; check before assuming

Deadlines

  • Register new facilities within 60 days of starting to manufacture or process cosmetics for the U.S.
  • Renew every 2 years
  • Update product listings annually

Steps

  1. Get a FEI number for the facility if you don't have one
  2. Prepare facility, responsible person and product category data
  3. Submit through FDA's Cosmetics Direct portal (or SPL)
  4. Name the U.S. Agent with their contact details
  5. Keep your facility registration number for product listings

Common mistakes

  • Confusing the "responsible person" (on the label) with the U.S. Agent
  • Missing the biennial renewal
  • Selling or buying "MoCRA certificates": FDA does not issue them

How US Agent Desk helps

We serve as your U.S. Agent, prepare the registration data in your language for your company's officer to submit, confirm the designation when FDA asks, and check FDA's public records for your company every morning. Prices start at $990 per year.

Check if you need a U.S. Agent See prices

Independent private service. Not affiliated with the U.S. FDA. Not legal advice.