The EU packaging regulation has applied since 12 August 2026. PFAS limits, an EU declaration of conformity, responsibility of the brand owner: here is what a food supplement brand needs to know and do now.

Regulation (EU) 2025/40 on packaging and packaging waste gradually replaces the former directive. It has applied since 12 August 2026. Unlike a directive, it applies directly in every Member State. For food supplements, it covers every format: jars, bottles, pouches, sticks, blisters, cartons and shipping boxes.
The key point lies in the definition of manufacturer. The guidance published by the Commission on 10 June 2026 states that a person who has packaging or a packaged product designed or manufactured under its own name or trademark is the manufacturer. The reason given: that person has the decisive power over its suppliers and can therefore set the characteristics of the packaging. In private label, the brand therefore bears legal responsibility for compliance.
Since 12 August 2026, packaging intended to come into contact with food can no longer be placed on the market if it exceeds any of these thresholds:
The Commission guidance recommends a stepwise approach: measure total fluorine first. Below 50 mg/kg, compliance is indicated. Above that, further analysis is needed. Inks, varnishes and adhesives on the packaging must also be taken into account.
Every packaging must be covered by an EU declaration of conformity, drawn up on the basis of technical documentation. The manufacturer within the meaning of the PPWR is solely responsible for it, even when a third party drafts it. Packaging and material suppliers must provide the information needed. Documentation must be kept for 5 years for single-use packaging and 10 years for reusable packaging.

The Commission guidance is clear: food-contact packaging placed on the market before 12 August 2026 can remain on sale, with no withdrawal required. However, any packaging placed on the market after that date must meet the PFAS limits. For a finished product, the right reflex is to check packaging compliance for every new production run.
On 9 September 2026, the European federation EHPM called for a pragmatic implementation for food supplements. It points out that stability studies often take 24 to 36 months, which makes packaging changes slow to validate, and asks in particular for a temporary derogation until 2035 on recyclability where no validated alternative exists.
Irati Production manufactures your brand's food supplements in France and supports you on regulatory compliance.
Regulation (EU) 2025/40 has applied since 12 August 2026. PFAS limits for food-contact packaging and the EU declaration of conformity have been required since that date.
According to Commission guidance, a person who has a packaged product made under its own name or trademark is considered the manufacturer of the packaging. In principle, that is the brand.
No. Food-contact packaging placed on the market before 12 August 2026 can remain on sale. Packaging placed on the market after that date must meet the PFAS limits.
25 ppb for any individual PFAS measured by targeted analysis, 250 ppb for the sum of those PFAS and 50 ppm for total PFAS, including polymers.
Yes. We manufacture your food supplements in France and our regulatory team checks formulas, labelling and claims. Contact us to discuss your project.
For information only, not legal advice. Sources: Regulation (EU) 2025/40 on packaging and packaging waste (PPWR); Commission Notice C/2026/3084, guidance document on Regulation (EU) 2025/40, published 10 June 2026 (eur-lex.europa.eu); LNE, PPWR PFAS thresholds for food packaging (lne.fr); SGS, 20 July 2026; NutraIngredients, 9 September 2026 (EHPM position).
Formula, packaging, label: we build with you a product ready for the European market.
Request a free quote