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HomeFood and BeveragesFCE (Food Canning Establishment) and SID (Process Filings)U.S. FDA FCE-SID Examples › Wild Ginseng Drink Regulations

U.S. FDA FCE-SID Wild Ginseng Drink Requirements



Food canning establishments in the United States and foreign establishments that process and export foods to the United States are subject to regulations that require registration of the establishments (FCE) and filing of scheduled processes (SIDs). The FCE registration and SID regulations for thermally processed low-acid and acidified foods packaged in hermetically sealed containers are found in Title 21 CFR 113 and 114. Typical hermetically sealed Wild Ginseng Drink products include:
  • Canned Wild Ginseng Drink
  • Bottled Wild Ginseng Drink
  • Jarred Wild Ginseng Drink
  • Wild Ginseng Drink in Pouch
  • Wild Ginseng Drink in Tetra Pak
  • Wild Ginseng Drink in Dressing
  • Marinated Wild Ginseng Drink
  • Wild Ginseng Drink in Water
  • Wild Ginseng Drink in Oil
  • Wild Ginseng Drink in Brine
  • Wild Ginseng Drink in Sauce
  • Wild Ginseng Drink in Syrup
  • Wild Ginseng Drink in Spring Water
  • Wild Ginseng Drink in Vinegar
Registrar Corp assists Wild Ginseng Drink companies with:
  • FDA Wild Ginseng Drink FCE Registration
  • FDA Wild Ginseng Drink SID Process Filing
  • FDA Wild Ginseng Drink FCE-SID Exceptions
  • FDA Wild Ginseng Drink Label Requirements
  • FDA Wild Ginseng Drink Import Information
  • FDA Wild Ginseng Drink Detentions / Wild Ginseng Drink Entry Refusals
  • General U.S. Food and Drug Administration Guidelines for:
    • Wild Ginseng Drink Manufacturers
    • Wild Ginseng Drink Suppliers
    • Wild Ginseng Drink Processors
    • Wild Ginseng Drink Exporters
    • Wild Ginseng Drink Importers
In addition to Wild Ginseng Drink Food Canning Establishment Registration (FCE) and Scheduled Process (SID) regulations, Wild Ginseng Drink businesses are typically subject to U.S. FDA Food Facility Registration and U.S. Agent requirements (when applicable). For more information about Wild Ginseng Drink requirements, simply choose one of the options below:




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U.S. FDA Regulations:

U.S. FDA FCE/SID: 21 C.F.R. sections 108, 109, 113, 114













Registrar Corp assists businesses with U.S. FDA compliance. Certificates of Registration issued by Registrar Corp provide confirmation to industry that you are fulfilling U.S. FDA registration requirements. U.S. FDA does not issue or recognize Certificates of Registration. Registrar Corp is not affiliated with the U.S. Food and Drug Administration.

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