BUSINESS NEWS
UPDATED: 10.08.2026
Products for the Swiss market are subject to a declaration obligation: they must include information about the party placing the product on the market, the price in Swiss francs, and quantity information. They must also be declared in at least one official language (German, French, or Italian), though in practice, they must be trilingual for nationwide distribution. The legal foundations for this are the Consumer Information Act (KIG), the Price Disclosure Ordinance, and the Product Safety Act (PrSG); EU markings do not apply automatically.
The linguistic scope follows a tiered principle. The legal minimum standard is a declaration in at least one official language. For safety- and health-related information, such as warning notices or allergens, a stricter standard applies, as this information must be unmistakable for consumers. Anyone selling nationwide across the German, French, and Italian language regions makes trilingual declaration (G/F/I) the de facto standard. Multilingual labeling is therefore not just a "nice-to-have" but a business necessity for cross-regional distribution.
Furthermore, the specific scope of duties differs by product category. For food, cosmetics, textiles, and technical and electronic products, additional specific labeling requirements apply on top of the basic information. At this point, a common misconception persists: that an EU-compliant label or an existing CE marking is automatically sufficient for Switzerland. This is not the case. Conformity marking based on the EU model does not make a product compliant with Swiss law, and even the new EU General Product Safety Regulation (GPSR) does not change this, as it does not apply directly to Switzerland as a non-EU market.
For expanding brands from the DACH region, this is not a mere formal detail but a specific financial and legal risk. Incorrect labeling can lead to a sales ban, legal sanctions, or a product recall, with immediate consequences for revenue and brand reputation. The responsibility for this lies with the party placing the product on the market—the person who first brings the product to the Swiss market. This system serves consumer protection and fair competition between providers. Anyone planning a successful export to Switzerland should therefore include labeling in their preparations early on, just as they would for legally compliant sales in Switzerland through established marketplaces.
In short: To label products in a legally compliant manner for Switzerland, you need a declaration in at least one official language (effectively in German, French, and Italian for nationwide sales), correct manufacturer information, price marking in Swiss francs, and the appropriate proof of conformity.
Correct labeling and declaration for the Swiss market can be divided into five specific implementation steps that every party placing products on the market can work through in order. This structure translates abstract requirements for product labeling into a clear sequence of actions ranging from linguistic scope to proof of conformity.
Ensure Multilingual Product Declaration: Provide mandatory information in at least one official language, and in German, French, and Italian for sales across multiple language regions.
Correctly Identify Manufacturer Information and Origin: State the name and address of the party placing the product on the market. An indication of provenance or origin is only necessary if prescribed or advertised, in which case it must be correct and not misleading.
Implement Price Disclosure and Quantity Information: Disclose the final price in Swiss francs including all taxes, supplemented by unit and quantity information.
Observe Industry-Specific Labeling Requirements: Fulfill additional requirements that apply depending on the product category, such as for food, cosmetics, textiles, or technical goods.
Provide Proof of Conformity and Technical Documentation: Maintain the required declarations of conformity and technical documents for regulated products.
The first three steps form the basic declaration obligations that apply to all goods. Industry-specific duties and proof of conformity—documents proving compliance with applicable safety requirements—are added depending on the product category. The responsibility for the full implementation of this declaration obligation lies in all cases with the party placing the product on the market.
Practical product declaration in Switzerland begins with the question of the extent to which mandatory information must be translated. The required linguistic scope depends on the product type and the sales region. While marketing copy allows for creative leeway, safety- and health-relevant information such as warnings or allergen declarations demand a significantly stricter standard. Labels purely in English or exclusively in other foreign languages are not sufficient for these safety-relevant details.
Multilingual labeling is thus oriented toward the protection needs of consumers. If you sell nationwide across all language regions, there is practically no way around a trilingual declaration in German, French, and Italian. Special attention is required for chemical products such as detergents or cosmetic raw materials: with the revised chemicals law, the principle of the official language of the place of supply will apply more strictly as of 2026. Purely bilingual labeling will then no longer necessarily suffice for nationwide distribution, as the labeling must be in the language of the region in which the buyer receives the product—for example, in Italian in the canton of Ticino.
For most products, the name and a reachable address of the party placing the product on the market must appear on the product itself or on its packaging. If the goods are imported, the importer or an authorized representative based in Switzerland takes this place. This information provides a clear point of contact for consumers and authorities and must be permanent, easily legible, and uniquely identifiable.
The situation is different for origin labeling. A statement of source or origin is generally not mandatory for most non-food products, whereas it is often mandatory for food. As soon as you actively promote a Swiss origin, the "Swissness" rules apply, and the statement must not be misleading. These rules are strictly quantified: for food, at least 80 percent of the raw material weight must come from Switzerland (100 percent for dairy products); for industrial products, at least 60 percent of the manufacturing costs, including research and development, must be incurred in Switzerland.
The Price Disclosure Ordinance (PBV) regulates how you must display prices to consumers. It requires the disclosure of the final price actually to be paid in Swiss francs, including value-added tax and all unavoidable surcharges. The consumer must be able to see at a glance what they will pay in the end. Specifically, this duty consists of three elements:
Final Price: The full retail price in francs including all taxes and surcharges.
Unit Price: For comparable products, additionally the price per unit of measurement, such as per kilogram or liter, so that consumers can compare offers.
Quantity Information: Quantity, weight, and volume indications must be correct and provided in metric units.
Beyond the basic duties, additional Swiss labeling regulations apply depending on the product range, the scope of which increases with the safety and health risks of the respective product category. The range spans from food, cosmetics, and textiles to technical products. Especially with a broad assortment, e-commerce brands often underestimate the effort required for cross-category compliance checks. Missing or incorrect assignment to industry-specific regulations is one of the biggest hurdles when entering the Swiss market and can noticeably delay a planned launch. Do not rely blindly on the Cassis-de-Dijon principle: it does not apply in every sector, which is why you must separately check the specific exceptions and registration requirements in Switzerland per category, such as cosmetics versus textiles.
For regulated products, especially technical and electronic ones, a declaration of conformity and the associated technical documentation must be available. The declaration of conformity is the document by which the party placing the product on the market bindingly confirms that a product meets the applicable safety requirements. The visible conformity marking on the product documents this compliance externally. You must be able to produce both types of proof upon request by the authorities, which is why you must archive and keep the documents accessible for the legally prescribed period.
The situation is particularly demanding for medical devices, systems, and in-vitro diagnostics. Since the Mutual Recognition Agreement for medical devices has effectively ceased to apply, EU approvals are no longer automatically valid in Switzerland. Manufacturers without their own Swiss headquarters must mandate a Swiss Authorized Representative, known as a CH-REP. This representative monitors registration requirements with the licensing authority Swissmedic and is locally liable.
Switzerland is not an EU member and has an independent legal system. This results in specific declaration obligations for products in Switzerland, the causes of which can be attributed to four central reasons. These factors work together to make a Swiss-specific adjustment of labeling necessary.
Deviations from EU Law: As a non-EU country, Switzerland does not automatically adopt EU requirements, which is why labels and proofs must be adapted.
Multilingualism as a Legal Requirement: The official languages regulation requires mandatory information in at least one official language and makes it multilingual for nationwide sales.
Consumer Protection and Fair Competition: Transparent labeling ensures informed purchasing decisions and prevents distortions of competition.
Product Safety Act as a Legal Foundation: The PrSG forms one of the central legal frameworks for product safety and labeling.
Switzerland does not automatically adopt EU law. Alignment occurs only partially through bilateral agreements and "autonomous implementation," where the legislator voluntarily and by its own decision converts EU rules into Swiss law. In practice, this partial alignment means there is no automatic equivalence between EU and Swiss conformity.
A clear example is the EU General Product Safety Regulation (GPSR), which does not apply directly to Switzerland. Similarly, an existing CE marking—the EU symbol for compliance with European safety requirements—does not automatically make a product compliant with Swiss law. Brands must therefore always check what additional adjustments are necessary beyond EU conformity, such as linguistic declarations or a Swiss contact person for certain product categories.
With German, French, and Italian, Switzerland has multiple official languages, which directly impacts labeling. Consumer information must therefore be available in at least one of these official languages, and practically in all three for nationwide distribution. The classification is key: for safety- and health-relevant information, multilingual labeling is not a voluntary service but is anchored in law. The required linguistic scope is consistently based on consumer safety and comprehensibility, not on business convenience.
Labeling requirements pursue a dual goal. On one hand, they serve consumer protection—the principle that buyers should be able to make informed purchase decisions based on complete and correct information. On the other hand, uniform requirements ensure fair competition: they prevent providers from gaining an advantage over correctly declaring competitors by using misleading or incomplete information. Transparency regarding origin, price, and content thus strengthens not only individual purchase decisions but trust in the Swiss market as a whole.
The Product Safety Act (PrSG) forms one of the central legal frameworks for placing safe products on the market in Switzerland. It obliges the party placing the product on the market to bring exclusively safe and correctly labeled products to market and is fleshed out by numerous ordinances. For the declaration of goods, the Consumer Information Act (KIG) and the Price Disclosure Ordinance apply additionally.
Beyond mere duties, the PrSG defines responsibilities and provides the basis for governmental market surveillance—the state control of whether products placed on the market meet legal requirements. This interplay of framework legislation and specific ordinances explains why Swiss labeling cannot be derived from a single regulation.
Specifically, which labeling requirement applies in Switzerland depends significantly on the product category. General basic duties exist for all goods, onto which additional specific requirements are built depending on the category. The scope of regulation increases with health and safety risks. Four categories are the primary focus.
General Labeling Requirements for All Goods: Basic information such as the party placing the product on the market, price, and quantity apply across all products; an origin statement only where prescribed or advertised.
Labeling Requirements for Food: Additional duties regarding ingredients, nutritional values, allergens, origin, and shelf life.
Labeling Requirements for Cosmetics and Textiles: Ingredient declarations, fiber content, and care instructions.
Labeling Requirements for Technical and Electronic Products: Conformity and safety markings as well as technical documentation.
This system shows that product labeling in Switzerland is not a uniform set of rules but is composed of cross-product basic duties and category-specific labeling obligations.
Regardless of category, certain information forms the foundation of every correct label. These basic duties are the base upon which all category-specific duties are built. Most goods should therefore include:
Responsible Party: Name and reachable address of the party responsible in Switzerland.
Price: The final price in Swiss francs.
Quantity: A correct statement of quantity, weight, or volume.
Origin: An origin marking only if prescribed or actively promoted.
All of this information must be permanent, easily legible, and provided in at least one official language.
Food labeling is among the most densely regulated areas, as the information here directly affects the health of consumers. It includes a series of mandatory details that go beyond the general basic duties:
Legal Name: The accurate description of the foodstuff.
Ingredient List: A full list of all ingredients in descending order of their weight proportion.
Allergens: Allergens must be highlighted and clearly declared in the ingredient list.
Nutritional Values: Disclosure of nutritional values per defined serving size.
Shelf Life: Best-before or use-by date and, if applicable, storage instructions.
Origin and Lot: Origin and lot information where prescribed for the respective product.
These details ensure that consumers can judge the composition and safety of a food item before purchase.
Cosmetics and textiles each follow their own labeling logics, which warrants separate consideration.
For cosmetics, ingredient declaration according to the INCI standard is mandatory—this is the international nomenclature for cosmetic ingredients ensuring uniform naming of components. Additionally, details on volume, shelf life, and usage instructions are required. It should be noted that the Cassis-de-Dijon principle has clear limits here: Swiss cosmetics law strictly requires a responsible person based in Switzerland to hold the Product Information File.
For textiles, the focus is on fiber composition—the precise stating of the textile fibers used and their proportions—as well as care instructions. Here, too, the Cassis-de-Dijon principle does not apply without restriction: textiles that do not meet specific Swiss requirements regarding flammability and combustibility may not be sold as is. Both categories must not be misleading, and safety-relevant information must be understandable to consumers.
Technical and electronic products are subject to one of the most demanding labeling regimes since they can pose increased safety risks. They require appropriate conformity markings and a declaration of conformity documenting compliance with applicable safety requirements. Supplementary duties include safety and warning instructions as well as complete technical documentation.
At this point, the deviation from EU law becomes particularly relevant. CE marking is EU-based and not automatically sufficient for Switzerland. A product that is marketable in the EU does not necessarily meet Swiss requirements. You must therefore ensure that Swiss-specific conformity is separately provided and documented.
Incorrect product labeling in Switzerland rarely goes without consequences. Those who violate Swiss labeling requirements must expect multi-stage consequences ranging from regulatory orders and sales bans to legal sanctions and product recalls. The severity of the consequences depends on the nature, risk, and recurrence of the violation. The responsibility for this lies primarily with the party placing the product on the market.
Regulatory Complaint: Market surveillance demands a correction of the labeling within a set deadline.
Sales Ban: Non-compliant products may no longer be sold, either temporarily or permanently.
Product Recall: Products already on the market must be retrieved.
Legal Sanctions: Violations of labeling and price regulations can lead to fines and other measures.
Competition Law Consequences: Misleading information can trigger cease-and-desist warnings and claims from competitors.
Reputational and Revenue Damage: The loss of trust among consumers and marketplaces leads to lost sales.
Yes. A sales ban is a real consequence if a declaration does not meet requirements. It is defined as a regulatory order to temporarily or permanently stop placing a product on the market. Market surveillance can sometimes issue such a ban immediately in the case of safety-relevant defects. Typically, however, it begins with a complaint and a deadline for correction. Only if a brand fails to react or if there is an immediate danger does a distribution stop follow. For sellers on Swiss marketplaces, a sales ban means an immediate stop to the affected listings and thus direct lost revenue.
Yes. Violations of labeling and pricing regulations can result in legal sanctions, meaning state-imposed fines and other regulatory measures. The amount depends on the severity, intent, and recurrence of the violation. The possible fines are substantial and clearly quantified by law: intentional violations of labeling duties and safety warnings can be punished with fines of up to 40,000 francs under the Product Safety Act. In the sensitive food sector, violations can even lead to fines of up to 80,000 francs. Additionally, there are possible competition law claims from third parties. Legal responsibility for correct labeling lies with the party placing the product on the market.
Yes. A product recall is possible and refers to the request to retrieve products already sold or delivered from the market and from consumers. It becomes particularly relevant when missing or incorrect information represents a safety risk or health hazard. A recall causes not only direct costs for logistics and replacement but also significant reputational damage. It is ordered either by market surveillance or voluntarily by the party placing the product on the market. The most effective protection against a recall is correct labeling from the start. However, such clean labeling requires that the underlying terms are clearly distinguished from one another.
Product labeling and declaration encompass all legally required information provided on or with a product. Anyone wanting to categorize Swiss labeling regulations can understand the framework through three aspects: the distinction between terms, the legal foundations, and the question of responsibility.
Distinction of Terms: Labeling refers to the visible marking, declaration to the mandatory information required by content and law.
Legal Foundations: KIG, PrSG, PBV, and supplementary ordinances form the legal framework.
Responsibility: The party placing the product on the market is liable for correct labeling and declaration.
The difference between product labeling and declaration is that the two terms describe different levels, even if they are often used synonymously in everyday life. Product labeling refers to the visible marking of a product, such as through labels, symbols, or marks. Declaration, on the other hand, refers to the informational content—often strictly prescribed by law—such as the ingredient list, components, or origin. In practice, they overlap, but they are viewed differently from a legal perspective. Simply put: labeling answers the question of how a product is marked, while declaration determines which specific contents must be stated.
The legal core is formed by the Product Safety Act (PrSG) and the Consumer Information Act (KIG), supplemented by a series of product-specific ordinances. These sets of rules interlock depending on the category and set the respective minimum details. Key foundations include:
Product Safety Act (PrSG): Framework law for placing safe products on the market.
Consumer Information Act (KIG): Foundation for the declaration of goods and services.
Price Disclosure Ordinance (PBV): Requirements for price marking to consumers.
Sectoral Ordinances: Such as the Food and Commodities Ordinance for specific product areas.
The PrSG acts as a safety net in the sense of a lex generalis: it legally applies whenever no specific sectoral ordinances exist for a product or when they have regulatory gaps, ensuring the protection of humans and the environment. Swiss requirements are independent and not identical to EU law.
The responsible party is the party placing the product on the market, i.e., the person who first introduces a product to the Swiss market. This can be the manufacturer, an importer, or an authorized representative based in Switzerland. This responsibility is comprehensive and extends to the accuracy, completeness, and up-to-date nature of all mandatory details.
For expanding brands from the DACH region, this point is of central importance. If you sell your products via Swiss marketplaces, you can legally be considered the party placing the product on the market and are thus directly responsible. Retailers and marketplace sellers also bear these duties as soon as they first place a product on the Swiss market. You should therefore clearly determine who will assume this role before market entry.
The legally compliant labeling for the Swiss market rests on a few but binding pillars: declaration in at least one official language (effectively German, French, and Italian for nationwide sales), correct manufacturer information, price marking in Swiss francs, as well as industry-specific duties and proof of conformity. The Swiss market requires independent labeling that cannot be derived from EU law. Legal certainty arises from the consistent fulfillment of the duties of the party placing products on the market; sales bans and recalls can be avoided through correct labeling from the start. A look at the categories shows how much requirements vary: food, cosmetics, textiles, and technical products each carry their own additional obligations.
For expanding DACH brands, a clear course of action can be derived from this. Before market entry, check which labeling your product category requires, adapt existing EU labels linguistically, switch price marking to Swiss francs, and have the necessary conformity documents ready. Specifically, this concerns preparing a marketplace listing, adapting existing EU labels, and building robust compliance documentation. Those who approach these steps structurally turn a perceived hurdle into a calculable process. Brands that do not wish to bear this administrative and legal complexity themselves will find SURS to be a one-stop-shop partner that handles the entire sales process across all relevant Swiss marketplaces without upfront costs, while also covering the requirements for labeling and conformity marking.
Mandatory details must be provided in at least one official language—German, French, or Italian. Those who sell their products nationwide across all language regions effectively declare in all three languages. The exact linguistic scope depends on the product type, the sales region, and safety-relevant information such as warning notices.
No. EU markings such as the CE mark are not automatically valid in Switzerland, as Switzerland is not a member of the EU. Products must additionally fulfill the independent Swiss labeling regulations, particularly the linguistic requirements for declaration and the Swiss-specific conformity of the respective product category.
The party placing the product on the market is liable, i.e., the person who first introduces the product to the Swiss market. This can be the manufacturer, an importer, or a Swiss authorized representative. Marketplace sellers can also be liable as soon as they themselves act as the party placing products on the market.
Yes. According to the Price Disclosure Ordinance, the final price must be stated in Swiss francs including value-added tax and all surcharges. For comparable products, the price per unit of measurement must additionally be disclosed. Exceptions to this unit price obligation exist for sales by piece count, for pre-packaged goods under a 2 franc retail price, and for high-priced products over 150 francs per kilogram for food or 750 francs per kilogram for non-food items.
Most products must display information about the party placing it on the market, the price in Swiss francs, and a quantity statement, provided in at least one official language and in a permanently legible form. Depending on the product category, specific mandatory details are added, such as origin and allergens for food products.
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