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Règles étiquetage produit cosmétique.

What do all these statements on a cosmetic product label actually mean?

As the first point of contact with the consumer, the label is the direct communication medium between a brand and its users. In Europe, cosmetic product labeling is not limited to displaying a name and a list of ingredients: it is about communicating in a legal, responsible, and transparent manner. As such, every label must be clear, legible, indelible, and easily understandable, and must contain a set of information defined and controlled by regulation. This article details all the requirements that brands must meet to comply with cosmetic product labeling rules in Europe.

Published on July 13, 2021, updated on April 10, 2026, by Stéphanie, PhD, Doctorate in Life and Health Sciences — 8 min of reading

Key points to remember about cosmetic product labeling rules.

  • Both in Europe and in the United States, thelabeling of a cosmetic product is subject to strict regulations. The information displayed on product labels enables consumers tomake informed choices when purchasing their products.

  • In accordance with regulations on cosmetic products, eight mandatory indications must appear on the label or packaging of any product placed on the European market: the contact details of the company marketing the product, the country of origin, the function of the product, the net quantity, the date until which the cosmetic product will continue to fulfill its original function, any necessary precautions for use and possible warnings, an identification reference, and the list of ingredients.

  • Any product whose labeling is incomplete or contains false or misleading statements may be subject to regulatory actions, ranging from withdrawal from the market to financial and legal penalties.

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What information must appear on the label of a cosmetic care product?

Cosmetic manufacturers are subject to strict regulatory requirements regarding labeling. Far from being a purely administrative constraint, these statements embody transparency, trust, and a brand’s credibility with its consumers. In Europe, they are governed by Regulation (EC) No. 1223/2009, whose objective is to harmonize practices among Member States to ensure consumer safety and fair competition.

This regulation defines a list of eight mandatory statements that must appear on the packaging of any cosmetic product placed on the European market. Failure to comply with the regulations on cosmetic product labeling renders a skincare product non-compliant, which can lead to various risks for companies, such as financial penalties, damage to their reputation, and legal action.

European regulations prohibit the use of claims (text, images, or other figurative signs) that attribute to cosmetic products characteristics or functions they do not possess, both on labeling and in advertising.

Beyond the content, the regulation also imposes requirements on the format of labeling. Above all, good labeling is labeling that is legible and accessible. This implies:

  • A clearly visible placement of essential information - this information must not be buried in a complex design or relegated among secondary elements.

  • Optimal legibility - adequate contrast, appropriate font size, indelible characters... the information must be written in a typeface adapted to the size of the container.

  • Respect for local languages - mandatory information must be written in the official language(s) of the country or countries where the product is marketed, in particular the product’s function and its precautions for use.

Well-designed labeling goes beyond mere regulatory compliance. It demonstrates transparency and professionalism, and can play a decisive role in the consumer’s purchasing decision.

When the space available on the packaging is insufficient to display all the required information, the precautions for use and the list of ingredients may appear on a separate medium (leaflet, folded label, attached card, etc.).

For brands, ensuring labeling compliance does not end with the initial drafting. Every graphic change or reformulation must undergo an updated regulatory review. The marketing and design teams involved in packaging creation must be trained in the applicable requirements (correct use of symbols, information hierarchy, mandatory warnings depending on product categories, etc.). Although Regulation (EC) No 1223/2009 does not set a minimum font size, a height of at least 1.2 mm is generally considered acceptable to ensure legibility.

Every product placed on the market, including samples, must comply with the Product Information File (PIF) and be documented in it, in accordance with the requirements of the regulation.

Information relating to the manufacturer.

The name or corporate name of the responsible person, that is, thenatural or legal person who guarantees, within the European territory, that the product complies with the regulations, must appear on the label, together with the address where the Product Information File (PIF) is available. This indication ensures the traceability of the product, transparency for consumers and establishes the legal liability of the manufacturer in case of any issue.

Lorsque le distributeur n'est ni le fabricant ni l'emballeur, cela doit être indiqué sur l'étiquette par une mention explicite du type "Fabriqué par…" ou "Distribué par…".

<h3>Information relating to the manufacturer

The country of origin of the product.

Indicating the country of manufacture is mandatory when its omission could mislead the consumer about the product’s actual origin. It fulfills legal and commercial requirements in terms of traceability and compliance with local standards, and prevents any risk of fraud regarding the place of production. For products manufactured within the European Union, this indication is not required.

<h3>The country of origin of the product

The intended function of the product.

Unless it is clearly deducible from the product name or design, indicating the product’s function is mandatory. Its purpose is to inform the consumer about the intended use and to avoid any confusion with other product categories. It must be written in the language of the country where the product is marketed. For example, a lipstick does not need to state that it is a “lip product,” because its function is obvious.

<h3>The intended function of the product

The nominal content.

The net content of the product at the time of packaging, expressed in weight (grams/pounds) or in volume (milliliters/ounces), is required in order to inform the consumer of the exact quantity being purchased. However, this statement is not mandatory for packages containing less than 5 g or 5 mL, free samples, and single-dose products.

<h3>The nominal content

The expiration date.

It corresponds to the limit up to which a product, when stored under appropriate conditions, fulfills its original function. It is expressed in two ways depending on the product’s lifespan:

  • The "Minimum Durability Date" (MDD) indicates up to what date an unopened product remains safe and effective. It is symbolized by an hourglass with the date next to it and preceded by the wording "Best used before…". Its indication is mandatory only when the product’s durability is less than 30 months.

  • The “Period After Opening” (PAO) specifies the number of months during which the product remains usable after it is first opened. It is represented by the pictogram of an open cream jar, with the duration in months written inside. The PAO only applies when the BBD (best before date) is longer than 30 months.

Certains produits ne nécessitent aucune de ces deux indications lorsqu'ils ne se détériorent pas dans des conditions normales d'utilisation. C'est notamment le cas des parfums et des aérosols.

<h3>The <a href="/library/how-is-the-expiration-date-of-a-cosmetic-product-defined" target="_self" linktype="story">expiration date</a>

The manufacturing batch number.

The batch number is a unique identifier assigned to a series of products manufactured under the same conditions (date, location, raw materials used, etc.). It enables precise traceability in the event of quality control, product recall, or regulatory investigation, and is an essential data point for health authorities in the event of an incident.

<h3>The manufacturing batch number

Precautions related to the use of the product.

Usage precautions indicate the best practices for using the product and help prevent misuse. Some are required by regulations, especially for products containing high‑risk ingredients or belonging to specific categories (aerosols, hair dyes, sunscreens, etc.), while others are recommendations specific to the brand.

<h3>Precautions related to the use of the product

The composition of the product.

It must be preceded by the term "Ingredients", and the INCI list (International Nomenclature of Cosmetic Ingredients) catalogs all of the ingredients that make up the product. This nomenclature is standardized internationally : the ingredient names are identical regardless of the language of the country where the product is sold, which makes it possible to objectively compare products marketed in different countries. This list allows consumers to know what they are applying, to identify the presence of any regulated allergens and to facilitate inspections by the competent authorities.

<h3>The composition of the product

The recycling logo.

The "Triman" logo, accompanied by sorting instructions, has been mandatory in France since January 1st 2015 for all household packaging. It indicates that the product or its packaging must be directed to a selective collection stream (in‑store collection bins, recycling centers, or curbside sorting bins) rather than disposed of with household waste. This logo is not required under European Regulation (EC) No. 1223/2009, but falls under national environmental regulations. Other European countries have their own requirements for environmental labeling, notably Germany and Italy.

<h3>The recycling logo

Are the labeling regulations the same in Europe as they are in the United States?

In the United States, cosmetic products are subject to regulation by the FDA (Food and Drug Administration), governed by the Federal Food, Drug, and Cosmetic Act (FD&C Act) and the Fair Packaging and Labeling Act (FP&L Act). All mandatory regulatory statements must be written in English. U.S. regulations distinguish two labeling panels on the packaging, for which the required information differs:

  • The "Principal Display Panel" (PDP) is the side most likely to be seen or examined by the consumer on the shelf. It must display the product name, its nature or intended use, and the net quantity.

  • The "Information Panel" (IP) includes the other sides of the package, such as the sides or the back of the secondary packaging — It must indicate directions for use, precautions for use, warnings, the name and address of the company, and the list of ingredients.

And what about voluntary claims related to cosmetic products?

Beyond the mandatory legal information, cosmetic packaging is often enriched withvoluntary claims added by brands to highlight specific characteristics of their products. These statements are regulated by Regulation (EU) No 655/2013, which establishes six common criteria that every cosmetic claim must meet: compliance with legislation, truthfulness, evidence that varies according to the nature of the claims, honesty, fairness, and enabling informed choice.

Useful claims but without any legal definition.

Certain terms—such as "organic," "natural," or "vegan" —are very common on labels, but they have no official definition under European cosmetics regulations. Their use is governed solely by private certification schemes (COSMOS, Ecocert, NATRUE, PETA, V-Label, etc.), whose specifications differ from one another. If no certifying body is clearly identified on the packaging, these claims are the sole responsibility of the brand.

Typology products are certified by the PETA label.

Claims that are prohibited because they are redundant with the law.

Certain claims are explicitly prohibited because they only restate a legal requirement that already applies to all products. This is the case for “not tested on animals”. Since 2013, animal testing has been banned in the European Union for cosmetics, both for ingredients and for finished products. Using this claim would suggest that other products placed on the European market are tested on animals, which is false and constitutes a misleading commercial practice under European law.

Claims permitted subject to supporting evidence.

Other statements are permitted, provided they are supported by evidence documented in the DPP:

  • The statement "tested under dermatological control" indicates that a skin tolerance test was carried out under the supervision of a dermatologist. It does not mean that the product is suitable for all skin types, nor that it is hypoallergenic. There is no standardized testing protocol or minimum panel size required by regulations.

  • The term "hypoallergenic" may be used provided that the brand can demonstrate that the formulation minimizes, as much as current scientific knowledge allows, the risk of allergic reactions. There is no regulatory European definition of this term, nor any shared threshold. Each brand applies its own criteria—often the exclusion of certain known allergens—without any requirement to disclose them publicly.

    This statement does not mean that a product is free from any risk of allergy, but rather that a formulation effort has been made in this direction, supported by documented evidence included in the Product Information File (PIF).

  • The label "non-comedogenic" indicates that a product is formulated to minimize the risk of clogging hair follicles. This claim must be supported by evidence, but the testing methods used (clinical evaluations, self-reported questionnaires) are not harmonized at the European level.

The claims "[substance name]-free," useful when they can be verified.

Claims such as “fragrance-free,” “alcohol-free,” “sulfate-free,” “silicone-free,” or “soap-free” can be directly verified via the INCI list: if the ingredient does not appear there, the claim is factually accurate. These claims are considered acceptable when they provide useful information to the consumer, particularly for reasons related to health, ethics, or specific lifestyles—for example, “fragrance-free” or “alcohol-free” for sensitive/reactive skin, or “sulfate-free” to help preserve hair color.

However, certain limits apply. On the one hand, it is forbidden to disparage a legally authorized ingredient. A “paraben-free” claim that implies that parabens authorized by regulation are dangerous would constitute unjustified denigration of a substance that has been assessed and regulated by European health authorities. On the other hand, non-verifiable claims are contrary to the criteria of Regulation No. 655/2013. This is the case, for example, for “free from endocrine disruptors,” for which there is no officially recognized definition, and for “free from allergens,” which is misleading — any substance can be a potential allergen for a person who is sufficiently sensitized.

Sources

FAQ on cosmetic product labeling.

Are the labeling rules the same for all types of cosmetic products?

The eight mandatory statements defined by Regulation (EC) No 1223/2009 apply to all cosmetic products without exception. For certain categories of products that present a particular risk profile, European regulations require additional, specific statements that are added on top of this common baseline.

  • Les soins solaires doivent intégrer des messages sur le bon usage du soleil. Certaines allégations y sont explicitement interdites, notamment toute mention suggérant une "protection totale" contre les UV, qui serait trompeuse.

  • Les teintures et colorations capillaires doivent indiquer que le produit "peut provoquer des réactions allergiques sévères", inviter le consommateur à lire et suivre les instructions d'utilisation, et recommander la réalisation d'un test préalable avant chaque application. Ces exigences visent à réduire le risque de sensibilisation, certains ingrédients de ces formules présentant un potentiel allergisant documenté.

  • Les dentifrices contenant du fluor destinés aux enfants doivent indiquer la concentration en fluorure exprimée en ppm (parties par million). Une mention "Ne pas avaler" et un avertissement recommandant de tenir le produit hors de portée des jeunes enfants sont également obligatoires.

Is a product sold online subject to the same labeling requirements?

Yes. Cosmetic products sold online in the European Union are subject to the same regulatory requirements as those sold in physical retail locations. The legal information must be accessible before purchase on the product page and present on the physical packaging delivered.

The INCI list is unreadable on my packaging. Is this legal?

In principle, no. Regulation (EC) No 1223/2009 requires that the information be indelible, easily legible, and clearly visible. A font that is too small or insufficient contrast may be considered non‑compliant. National regulatory authorities may impose sanctions for labeling that is deliberately illegible.

Can we rely on the date printed on a product if the packaging is damaged or the product has been exposed to heat?

No. The BBD and PAO are only valid under appropriate storage conditions — protected from heat, moisture, and direct light. A product exposed to unfavorable conditions may degrade before its expiration date. If there is any change in texture, odor, or color, it is best to stop using the product, regardless of the date shown on the packaging.

Do all cosmetic products have to be equipped with a tamper-evident device?

There is no mandatory requirement on this matter in European regulations. For most cosmetic products, the decision to add a tamper-evident device (such as a peel-off or adhesive seal, a tear strip that breaks on opening, a sealed box, a breakable cap, etc.) is part of a voluntary quality approach by the brand, based on its assessment of the risks related to product safety and storage conditions. However, certain intimate hygiene and oral hygiene products must be packaged in tamper‑evident containers for retail sale. If this device is missing or broken, the consumer must be able to detect it.

Are non-prepackaged products also subject to labeling regulations?

Non-prepackaged products, that is, those packaged at the time of sale such as certain products sold in bulk, must also comply with the labeling regulations in force in the Member States. The mandatory information must be accessible to the consumer before or at the time of purchase.

Do the inner label and the outer packaging have to contain the same information?

As a general rule, yes. The information required on the inner label, affixed directly to the container, is the same as that appearing on the secondary packaging (cardboard box, case, etc.). However, the list of ingredients may be omitted from the container if it already appears on the outer packaging.

En l'absence d'emballage extérieur, comme pour un baume à lèvres vendu sans boîte, le contenant doit à lui seul comporter toutes les mentions obligatoires.

What does the “open book” symbol sometimes found on certain products mean?

This pictogram indicates that certain mandatory information is available in a supplementary format (leaflet, web page accessible via a QR code, etc.). It is used in particular for mini-sizes (5 mL or less) or products with special shapes.

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