Do I need FDA registration for empty plastic bottles exported to the U.S. for cosmetics ?

It is simply a plastic bottle and cap for cosmetics, and the FDA does not require registration. However, the FDA has regulatory requirements for such products. However, if it is used to package drugs and medical devices, it is necessary to file for DMF and MAF.

In addition, cosmetics are also required to file FDA declarations for special major pigment batches. Click here for a free overview of FDA regulatory requirements

Food and Drug Administration (FDA) in charge: supervision and inspection of food, drugs (including veterinary drugs), medical devices, cosmetics, and electronic products; Testing, inspection and certification of ionic and non-ionic radiation generated during the use or consumption of products that affect human health and safety.

According to the regulations, the above products must be certified safe by FDA inspection before they can be sold on the market. The FDA has the right to inspect factories and prosecute violators.

Need! Although the brother above said it is too simple, hehe, in fact, it is as simple as that.

It is recommended that you ask your buyer to find a local logistics and freight company who is familiar with the local customs, and they can help you get it. You don't have to be busy, that's not something that our national logistics freight forwarding company can do!

Purely plastic bottles and caps also need FDA certification, no importer is required to provide, only the exporter (you) to provide.

As for the unwanted method, I think you should negotiate with your customers in the United States, and you can't trespass without permission, the consequences are very serious, and the United States is very angry.

Yes, if it is exported as a commercial product, authorization is required. Otherwise, it will be returned.

If it does not meet the requirements, do not ship directly, the customer is urgent, and it will be detained at that time.

If you want to come out directly, SGS is only responsible for the incoming sample, and you can find a suitable sample for him to test. However, this does not change the results of random inspections at the port of entry.

This takes time, and it can't be done in 3 months!

We used to have a customer who asked for FDA certification for food fillers

After arriving, the FDA test could not be carried out, and it was directly returned

The FDA for cosmetics is divided into testing and registration, and the premise of registration is that it must be a factory to complete FDA registration. General customs inspection is to check FDA registration, the recent inspection is stricter, if the value of the goods is relatively high, it is not recommended to take the risk of shipping.

It is possible that you will not be able to enter the customs, and you may be destroyed and fined!

This piece can be communicated, and we have made this piece specially.

We can handle FDA registration and FDA testing of cosmetics with a cycle of 5-7 working days.

I've been exposed to a little bit of this stuff before. For things like tea, the FDA registration number is only required for export. There doesn't seem to be a test standard.

Generally speaking, the import access of the United States is relatively strict compared to other countries, so as long as you obtain the information required by the United States to import such items, you can travel around the world. Personal opinions may not be absolutely accurate, and detailed documents need to be like a note from the certification department. 。

If you're satisfied, don't forget to take it.

Cosmetics import operation process:

Registration and filing with the Ministry of Health (receiving unit: Health Supervision Center of the Ministry of Health);

Production of Chinese labels (before April 2006, it was necessary to file with the General Administration of Quality Supervision and Inspection, and the filing has been cancelled);

customs clearance (including label review, customs);

Listed for sale. Information required for the import of cosmetics:

1) Application form for the filing of imported non-special-purpose cosmetics;

2) product formula;

3) Product quality standards;

1. Inspection application form;

2. Notice of inspection acceptance;

3. Product manual;

4. Hygiene (microbiology, physical and chemical) test report;

5. Toxicological safety test report.

5) The original packaging of the product (including the product label). If the packaging is designed for the Chinese market to be marketed, the product design packaging (including product labels) must be provided at the same time;

6) Proof that the product is allowed to be produced and sold in the country (region) or country (region) of origin;

7) Letter of commitment on issues related to "mad cow disease";

8) If the declaration is made, the certificate of entrustment shall be provided;

9) Other materials that may be helpful for review.

Customs declaration of imported cosmetics requires the provision of Chinese labels, goods entry inspection and quarantine clearance form, product ingredient list, contract, invoice, packing list, inspection declaration, customs declaration power of attorney and other procedures.

The regulations issued by the FDA are an important part of the implementation of the Federal Food, Drug, and Cosmetic Act, and some of them are particularly important, such as: the current regulations on good manufacturing practices, which impose many requirements on hygiene, raw material inspection, finished product inspection, and other quality control. FDA food standards have specific requirements for many food products.

These regulations help both consumers and factories by telling them how they can guarantee that their products are qualified.

Cosmetics exported to the United States need to be registered with the FDA for customs clearance.

1. FDA registration: many products sold to the United States need to be registered (such as food, drugs, medical devices, laser products, etc.), and some products must be tested before they can apply for registration;

2. FDA testing: it is to test the product in accordance with FDA regulations;

The U.S. Food and Drug Administration (FDA) is one of the executive agencies established in the United States within the Department of Health and Human Services (DHHS) and the Department of Public Health (PHS). As a scientific governing body, the FDA's role is to ensure the safety of food, cosmetics, drugs, biologics, medical devices, and radiological products manufactured or imported into the United States. It was one of the first federal agencies to have consumer protection as its primary function.

Welcome to it.