FDA

FDA Regulated Products and Import Requirements

How to import cosmetics/beauty products into the US

Importing FDA Regulated Product & Compliance Consulting

Importing FDA-Regulated Products into the US

Welcome to our web page on how to import FDA-regulated products into the United States! Here, we will provide you with all the necessary information you need to know about importing FDA-regulated products, what it means, and how it works.

What Are FDA-Regulated Products?

FDA-regulated products are those that are subject to regulation by the U.S. Food and Drug Administration (FDA). These products include foods, dietary supplements, drugs, medical devices, cosmetics, and tobacco products. If you are planning to import any of these products into the United States, you need to be aware of the regulations and requirements set by the FDA.

Importing FDA-Regulated Products into the US

Importing FDA-regulated products into the United States can be a complex process, involving several steps and requirements. Here are some general steps to follow to ensure a successful import:

Step 1: Determine if Your Product is FDA-Regulated

The first step in importing FDA-regulated products into the US is to determine whether your product falls under the jurisdiction of the FDA. You can check the FDA's website to see if your product is regulated. If your product is regulated, you will need to comply with FDA requirements for importation.

Step 2: Obtain FDA Registration and Listing

To import FDA-regulated products into the US, you must be registered with the FDA as an importer. You will also need to list the products you plan to import with the FDA. This can be done through the FDA's Electronic Registration and Listing System (FURLS).

Step 3: Obtain Prior Notice of Importation

You will need to provide the FDA with prior notice of any shipment of food for humans and animals that you plan to import. This notice must be submitted electronically through the FDA's Prior Notice System Interface (PNSI), at least 15 calendar days before the anticipated arrival of the shipment.

Step 4: Comply with FDA Labeling Requirements

All FDA-regulated products that are imported into the US must comply with the FDA's labeling requirements. The labeling must include information such as the product name, manufacturer's name and address, ingredient statement, nutrition information (if applicable), and any required warning statements.

Step 5: Comply with FDA Import Requirements

In addition to the above steps, you must also comply with FDA import requirements. These requirements include inspections, sampling, and analysis of products at the port of entry to ensure they meet FDA regulations. Some products may also require specific import permits or certifications.

Conclusion

Importing FDA-regulated products into the US can be a complex process that requires compliance with a variety of regulations and requirements. By following the steps outlined above, and working with a qualified customs broker or logistics provider, you can ensure a successful import of your products. If you are considering importing FDA-regulated products, make sure to do your research, and consult with experts to ensure compliance with all necessary regulations and requirements.

In-Depth Coverage: Country of Origin

Importing FDA-Regulated Products: The Import Process

Customs Brokerage & Consulting

When goods are imported into the United States, in almost all cases, the goods are required to be “entered,” that is, declared to the U.S. Customs and Border Protection (CBP), and are subject to examination by CBP.

We help your goods clear quickly and efficiently with our electronic Automated Commercial Environment (ACE) and Automated Broker Interface (ABI) Single Window System.

We will review your documents and goods to ensure compliance with all laws and regulations enforced by the U.S Customs, FDA, USDA, EPA, and other Partner Government Agencies, while evaluating options for duty reductions.

Food Safety Compliance

Importers have an explicit responsibility to verify that their foreign suppliers have adequate preventive controls in place to ensure that the food they produce is safe. As Preventive Controls Qualified Individual (PCQI) in Preventive Controls for Human Food and Qualified Individual in Intentional Adulteration (IA) Rule for Food Defense Plan, we offer consulting services to help your business stay in compliance with the FDA Food Safety Modernization Act (FSMA). Read more…

In-Depth Coverage: Importing Medical Device

Medical Device

All medical devices imported into the United States must meet the regulatory requirements of both the U.S. Customs and FDA. Foreign manufacturers must meet applicable United States medical device regulations in order to import devices into the U.S. We support our clients to meet applicable medical device regulations in order to import devices into the U.S. Read more…

Label and Labeling Compliance

The FDA has primary responsibility for claims on product labeling while the FTC has primary responsibility for claims in advertising. We review your labeling and label claims for food and dietary supplements, medical devices, other regulated products to insure compliance with all laws and regulations enforced by FDA and FTC. Read more…

Logistic Solution

We can help you manage your import and export business. Our partners in Freight Forwarding and Logistics are very experienced in Air and Ocean Freight, Inland Transportation, Warehousing and Distribution. To move your cargo from its current location through customs to its final destination we will partner with you to find the best logistics solution for your business. Read more…

What Does FDA Regulate?

FDA-Regulated Products and Import Requirements

Design your own logistics

To move your cargo from its current location through customs to its final destination we will partner with you to find the best logistics solution for your business.

Customs Clearance and Import Requirements

FDA Compliance Guide

FDA Import Requirements

All products regulated by the Food and Drug Administration (FDA) must meet the same requirements, whether imported from abroad or produced domestically. The FDA determines whether products are admissible into U.S. commerce. FDA has jurisdiction over imported products at the time of entry but also after the products have entered domestic commerce. Read more…

Entry Review for FDA-Regulated Products

The FDA regulates a wide range of products, including foods, human and veterinary drugs, vaccines and other biological products, medical devices intended for human use, radiation-emitting electronic products, cosmetics, dietary supplements, and tobacco products. Each FDA-regulated commodity is subject to specific regulations, which you should be aware of when importing products into the United States. Read more…

Country of Production and Country of Origin

Food in Natural State: For food that is in its natural state, the FDA Country of Production is generally the country where the food was grown or collected, including harvested and readied for shipment to the U.S.

Food not in Natural State: For food that is no longer in its natural state, the FDA Country of Production is generally the country where the food was made or processed. However, if the article is made from wild fish aboard a vessel, the FDA Country of Production is the country in which the vessel is registered. Read more…

Personal Importation of FDA-Regulated Products

If you are entering the United States with FDA-regulated products in personal baggage or sending products by mail or courier from abroad, the FDA has guidance that governs personal importations. Personal importation is a product not for further sale or distribution into U.S. commerce. These products may be carried in baggage or shipped by courier or international mail. Read more…

In-Depth Coverage: Marketing and Advertising Compliance

International Mail Facility (IMF) and FDA

Mail entering the U.S. from abroad arrives at a U.S. Postal Service (USPS) sorting facility (International Mail Facility, IMF). Upon initial screening at arrival, USPS sends packages to U.S. Customs and Border Protection (CBP) for examination. CBP then refers the FDA regulated products to the FDA's investigators for review. Read more…

Import for Export of FDA-Regulated Products

Import for Export (IFE) allows for the importation of a product that is unapproved or otherwise does not comply with FDA laws and regulations if it is coming into the U.S. for further processing and ultimately exported out of the U.S. Read more…

Foreign Trade Zone (FTZ) and FDA

Because FTZs are considered to be outside the Customs territory for the purpose of Customs duties and Customs entry procedures, the import provisions of the Federal Food, Drug, and Cosmetic (FD&C) Act are not applied to foreign products brought into the FTZ. This means that FDA does not determine the admissibility of products brought into the FTZ; rather, FDA will make an admissibility decision when products are withdrawn from the FTZ for consumption. Although FDA does not make an admissibility decision when products are brought into the FTZ, FDA does still have jurisdiction over those products. Read more…

In-Depth Coverage: Importing Food Products

Food Safety Modernization Act (FSMA)

The FDA Food Safety Modernization Act (FSMA) enables FDA to focus more on preventing food safety problems rather than relying on reacting to problems after they occur. Read more…

Foreign Supplier Verification Program (FSVP)

Under the Foreign Supplier Verification Programs (FSVP) regulation, a U.S.-based importer is now required, among other things, to conduct a hazard analysis – an evaluation of risk of the food and foreign supplier – and to conduct verification activities based on the hazard analysis. Read more…

Preventive Control for Human Food

The preventive controls final rules require that a facility verify that hazards are being controlled and take corrective action to prevent contamination. Product testing and environmental monitoring are examples of steps that a company may take for the preventive controls. Read more…

Preventive Control for Animal Food

The Preventive Control for Animal Food (PCAF) rule applies to food for animals other than man. This includes, but is not limited to, companion (pet) animals, such as dogs, cats, and horses; and food-producing animals, such as cattle, pigs, and chickens. This also includes wild animals and minor species such as wild birds, deer, fish, hamsters, and honeybees. Read more…

Produce Safety

The Produce Safety Rule establishes mandatory science-based, minimum standards for the safe growing, harvesting, packing, and holding of fruits and vegetables grown for human consumption. These standards are designed to work effectively for food safety across the wide diversity of produce farms. Read more…

Protect Food against Intentional Adulteration

The Food Safety Modernization Act (FSMA) final rule “Mitigation Strategies to Protect Food Against Intentional Adulteration (IA rule)” is aimed at preventing intentional adulteration from acts intended to cause wide-scale harm to public health, including acts of terrorism targeting the food supply. Read more…

Understanding Food Import Regulations and Requirements

Under the Federal Food, Drug and Cosmetic (FD&C) Act, importers of food products into the U.S. are responsible for ensuring that the products are safe, sanitary, and labeled according to U.S. requirements. Read more…

Food Facility Registration

The Public Health Security and Bioterrorism Preparedness and Response Act of 2002 (the Bioterrorism Act) requires domestic and foreign facilities that manufacture, process, pack or hold food for human or animal consumption in the United States to register with the Food and Drug Administration (FDA). Read more…

Prior Notice of Imported Foods

The Bioterrorism Act requires that FDA receive prior notification of food, including animal feed that is imported or offered for import into the United States. Advance notice of import shipments allows FDA, with the support of the U.S. Customs and Border Protection (CBP), to target import inspections more effectively and help protect that nation's food supply against terrorist acts and other public health emergencies. Read more…

In-Depth Coverage: USDA-Regulated Products

Dietary Supplement

The law defines dietary supplements in part as products taken by mouth that contain a “dietary ingredient.” Dietary ingredients include vitamins, minerals, amino acids, and herbs or botanicals, as well as other substances that can be used to supplement the diet by increasing the total dietary intake; or a concentrate, metabolite, constituent, extract, or combination of the preceding substances. Read more…

Acidified and Low-Acid Canned Foods (LACF)

Acidified food (AF) and low-acid canned food (LACF) are subject to special control by the FDA, which are implemented through Food Canning Establishment (FCE) regulations and Scheduled Process Identification (SID) filings. Read more…

Label Claims for Food and Dietary Supplement

Food labeling is required for most prepared foods, such as breads, cereals, canned and frozen foods, snacks, desserts, drinks, etc. Among the claims that can be used on food and dietary supplement labels are three categories of claims that are defined by statute and/or FDA regulations: health claims, nutrient content claims, and structure/function claims. Read more…

Food and Generally Recognized As Safe (GRAS)

Certain food ingredients, such as those that are considered “generally recognized as safe” (GRAS) by scientific experts, do not require premarket approval as a food additive. Any substance that is reasonably expected to become a component of food is a food additive that is subject to premarket approval by FDA unless the substance is generally recognized as safe (GRAS). Read more…

Importing Animal Feeds and Pet Foods

Animal feeds and pet foods imported into the United States must be composed entirely of ingredients judged acceptable for use in such products. The FDA’s regulation of pet food is similar to that for other animal foods. The regulation requires that all animal foods, like human foods, be safe to eat, produced under sanitary conditions, contain no harmful substances, and be truthfully labeled. Read more…

In-Depth Coverage: Importing Cosmetics

Cosmetics

Importing Cosmetics into the U.S

Companies and individuals importing products considered to be solely cosmetics are not required to register with FDA, and a registration number is not required for importing cosmetics into this country. Read more…

Cosmetics – Regulations and Enforcement by FDA

Cosmetic products and ingredients, other than color additives, do not need the approval of the FDA before they go on the market in the U.S. However, the FDA can pursue enforcement action against products on the market that are not in compliance with the law, or against firms or individuals who violate the law. Read more…

Shelf Life and Expiration Dating of Cosmetics

The law does not require cosmetics to have an expiration date. However, manufacturers are responsible for making sure their products are safe. FDA considers determining a product’s shelf life to be part of the manufacturer’s responsibility. Read more…

Voluntary Cosmetic Registration Program (VCRP)

FDA encourages both domestic and foreign cosmetic firms to register their establishments and file Cosmetic Product Ingredient Statements with Voluntary Cosmetic Registration Program (VCRP), but as its name indicates, participation in this program is voluntary, not mandatory. VCRP applies only to cosmetic products being sold to consumers in the U.S. Read more…

Cosmetics, Drugs, and Combination Products

Classification of products as cosmetics, drugs, or cosmetics and drugs is a concern for manufacturers, as cosmetics are not subject to the same approval, regulatory, or registration requirements as drugs. In addition to saving considerable time and expense, this distinction allows manufacturers of products that are only cosmetics and not drugs or combination products to market their products with less regulatory oversight. Read more…

Cosmetics: Cruelty-Free or Not Tested on Animals

Some companies promote their products as not having been tested on animals, either because they contain all-natural ingredients or by labeling with such terms as “finished product not tested on animals,” “no animal ingredients,” or “cruelty free.” The law does not require cosmetic labeling to have FDA approval before cosmetic products go on the market, and the FDA does not have a list of approved or accepted claims for cosmetics. Read more…

Organic Labeling Claims on Cosmetic Products

As with many statements made on cosmetic products, the terms “natural” and “organic” have no specific definition in the Federal Food, Drug, and Cosmetic (FD&C) Act, which may lead to consumer confusion. While the FDA has authority for labeling of cosmetics, the agency does not regulate the use of the term “organic”— rather, the U.S. Department of Agriculture (USDA) regulates “organic” claims on cosmetic products. Read more…

Medical Device

Medical Device – Import Process

Foreign manufacturers must meet applicable U.S. medical device regulations in order to import devices into the U.S. even if the product is authorized for marketing in another country. In addition, foreign manufacturers must designate a U.S. agent. As with domestic manufacturers, foreign manufacturing sites are subject to FDA inspection. Read more…

Medical Device – Facility Registration and Device Listing

Owners or operators of places of business (also called establishments or facilities) that are involved in the manufacture, preparation, propagation, compounding, assembly, or processing of medical devices intended for human use in the United States are required to register annually with the U.S. Federal Food and Drug Administration (FDA). This process is known as establishment registration. Read more…

Premarket Requirements for Imported Medical Devices

If your product is labeled or used in a manner that meets the definition of medical device it will be regulated as a medical device and is subject to the FDA’s laws and regulations before, during, and after it is offered for sale or use in the United States. If you have classified your medical device you should select and prepare the appropriate premarket submission, if one is required for your specific product’s classification. Read more…

In-Depth Coverage: Importing Medical Device

Radiation-Emitting Electronic Product

Radiation-emitting Electronic Products

There are hundreds of electronic radiation-emitting products, including TVs, microwave ovens, DVD or Blu-ray players, and cell phones and wireless devices. And most hospitals have a variety of diagnostic x-ray systems, surgical lasers, ultrasound machines, maybe magnetic resonance and radiation therapy systems as well. All these radiation-emitting products are FDA regulated. Read more…

Tobacco

Imported Tobacco Products

Tobacco products imported or offered for import into the United States must comply with all the applicable requirements of the FDA’s laws and regulations. FDA also regulates electronic nicotine delivery systems (such as e-cigarettes and vape pens), all cigars, hookah (waterpipe) tobacco, pipe tobacco and nicotine gels, among others. Read more…

Combination Products

A combination product is a product composed of two or more different types of medical products (i.e., a combination of a drug, device, and/or biological product with one another). As technological advances continue to merge product types and blur the historical lines of separation between medical products, the FDA expects to receive large numbers of combination products for review. Read more…

Drug

Importing Veterinary Drugs

All veterinary drug products offered for import into the U.S. must have an approved new animal drug application (NADA), conditional approval, or index listing. The only exceptions to these requirements are when there is a drug shortage or the drug is considered to be medically necessary and an approved version is not available in the U.S. Read more…

Importing Biological Product

Biological and related products regulated by the FDA include blood and blood products, vaccines, allergenics, tissues, cellular and gene therapies, and medical devices involved in the collection, processing, testing, manufacture and administration of licensed blood, blood components and cellular products. Read more…

Importing Drugs into the United States

Almost any ingested or topical or injectable product that, through its label or labeling (including internet websites, promotional pamphlets, and other marketing material), is claimed to be beneficial for such uses will be regulated by FDA as a drug. The definition also includes components of drugs, such as active pharmaceutical ingredients. Read more…