MIXER & PACK SETS THE COURSE FOR USA

The designer, developer and manufacturer of perfumery and air fresheners for third parties is ready to conquer the American market with the FDA approval as private label manufacturer to operate in the United States.

26th february 2024 (Cabanillas del Campo, Guadalajara)

The developer of perfumery and air fresheners for private label obtains FDA approval under MOCRA to offers its services in the US market.

With the entry into force of the new Modernatization of Cosmetic Regulation Act (MOCRA) in the United States, one of the main changes is all manufactures of cosmetic products must registered with the Food & Drugs Administration (FDA). This registration was previously voluntary and now, with a few exceptions, has become mandatory for manufacturing companies, and the perfume manufacture Mixer & Pack, always at the forefront of all international changes, has already received confirmation from FDA, which means that its facilities are now registered to operate in the United States, facilitating entries market of its customer’s products.

According to data from the Instituto de Comercio Exterior (ICEX), the American market is the market that imports the largest quantity of beauty products from Spain. That said, the manufacturer of perfumery and cosmetics for private label, and in line with its strategy of growth in international markets, has opted to be at the forefront of the regulatory needs of such an important market for the Spanish beauty industry.

Among others, this new law requires: registration of facilities, listing of products, adverse effects, record keeping, product safety, new labelling requirements in addition to the current ones, labelling of the list of allergens in fragrances, company audits…

Mixer & Pack ́s Regulatory Affairs Department is working on upcoming changes, so in June 2023 it attended and open FDA consultation with the cosmetic companies from around the world, where the agency explained that is developing regulations to establish a Good Manufacturing Practice (GMP) standard for facilities that manufacture or process cosmetic products distributed in United States, while European companies told the agency about possibility of aligning efforts the UNE-EN ISO 22176 GMP Standard, which is the most widely used in the most counties.

Facilities Mixer & Pack.
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