Luxury Cosmetic Packaging, Built for Compliance

Absolutely. We use Pantone-matched spot colors with spectrophotometer verification to achieve Delta E values under 1.5. We provide physical color drawdowns for approval before production begins and maintain your color profiles for future orders.

Yes. Our eco-friendly options include FSC-certified papers, post-consumer recycled board, soy-based inks, biodegradable lamination alternatives, and kraft-based luxury packaging. We help brands achieve premium presentation with sustainable materials.

Under FDA 21 CFR Part 701, cosmetic labels in the US must include: (1) identity statement on the principal display panel, (2) net quantity of contents, (3) ingredient list in descending order of predominance using INCI names, and (4) manufacturer/distributor name and address. We review all cosmetic artwork against these requirements before production and can flag compliance gaps before plates are made.

The EU Cosmetics Regulation (EC) 1223/2009 requires labels to include: product function, list of ingredients using INCI nomenclature, nominal content, best-before or PAO (period after opening) symbol, precautions, batch code, and country of origin. Labels must be in the language(s) of the country of sale. We support multi-language labeling on a single label sheet or booklet format for EU multi-market distribution.

We offer hot foil stamping (gold, silver, rose gold, holographic), cold foil, embossing, debossing, spot UV, full-cover lamination (matte, gloss, soft-touch, silk), and varnish options. For luxury skincare boxes we also offer linen texture, velvet lamination, and custom CMYK + 2 PMS spot colour printing. All finishes are available from 500 units.

Key requirements per FDA 21 CFR Part 701 include: statement of identity, net quantity of contents, ingredient declaration in descending order of predominance, name and place of business, and any necessary warning statements. Our pre-press team reviews all artwork for compliance.

We maintain expertise in major regulations like EU 1223/2009 (including CPNP notification), Health Canada, and others. We guide clients on regional specifics, such as INCI ingredient nomenclature and symbol requirements, and produce market-specific versions from our integrated facility.

Yes. We use waterproof, oil-resistant face stocks and permanent adhesives tested for cosmetic environments. Our specialty materials, like synthetic papers and coated films, ensure legibility and adhesion remain intact on containers for creams, serums, and other formulations.

We guarantee your packaging meets all mandatory statements under FDA 21 CFR Part 701, including: correct ingredient listing in descending order of predominance, a conspicuous net quantity of contents, the identity of the product, and the name and place of business. Our pre-press checks ensure font size, legibility, and placement are fully compliant.

For EU compliance under Regulation 1223/2009, we manage the specific requirements such as listing ingredients per the INCI nomenclature, including the 'period after opening' (PAO) symbol, and ensuring all mandatory information is present in the required languages on the container and any outer packaging.

Absolutely. We use specialty materials like waterproof synthetic papers, BOPP films, and UV-cured coatings designed to resist abrasion, oil migration, and moisture. This ensures all cosmetic product labeling requirements for durability are met, keeping information legible and your brand looking pristine throughout the product's lifecycle.