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Detailed rules on the packaging and labelling of environmentally hazardous substances and preparations

Original Language Title: Nadere regels verpakking en aanduiding milieugevaarlijke stoffen en preparaten

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Detailed packaging and designation of environmentally hazardous substances

The Secretary of State for Welfare, Public Health and Culture, the Minister for Housing, Spatial Planning and the Environment, and the Secretary of State for Social Affairs and Employment;

Having regard to Article 36, third and fourth paragraph, of the Environmental Hazardous Substances Act (Stb. 1985, 639) and 6, first paragraph, point (b) and second paragraph of the Decision on packaging and labelling of environmentally hazardous substances (Stb. 1987, 516);

Decisions:


Paragraph 1. General

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Article 1

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For the purposes of this arrangement:

a. Law:

Environmental Environment Act ;

b. Decision:

Packaging and labelling of environmentally hazardous substances and preparations ;

c. Substance Directive:

Directive No 67 /548/EEC of the Council of the European Communities of 27 June 1967 on the approximation of laws, regulations and administrative provisions relating to the classification, packaging and labelling of dangerous substances (PbEG L 196);

ed. Preparations Directive:

Directive No 1999 /45/EC of the European Parliament and of the Council of the European Union of 31 May 1999 on the approximation of the laws, regulations and administrative provisions of the Member States relating to the classification, packaging and labelling of dangerous substances Preparations (PbEG L 200);

e. Plant protection products Directive:

Directive No 91 /414/EEC of the Council of the European Communities of 15 July 1991 concerning the placing of plant protection products on the market (PbEG L 230);

f. Regulation (EC) No 1272/2008:

Regulation (EC) The European Parliament and the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures, amending and repealing Directives 67 /548/EEC and 1999 /45/EC, and amending Regulation (EC) No 1272/2008 of 16 December 2008 on the classification, labelling and packaging of substances and mixtures. (PbEU L 353).


Paragraph 2. Stoffs

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Article 2

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Hazards related to the use of the substance as referred to in Article 1 (1), first paragraph, part day, of the Community-VOC-Directive on the application of the Provisions for the Decisionto implement The following definitions shall apply to the risks referred to in Parts 2 to 5 of Annex I to Regulation (EC) No 1408/71. 1272/2008.


Article 3 [ Expired by 01-12-2010]

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Article 4 [ Expired by 01-12-2010]

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Article 5 [ Expired by 01-12-2010]

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Article 5a [ Expaed by 01-12-2010]

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Article 5 (b) [ Expired by 01-12-2010]

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Article 6 [ Expired by 01-12-2010]

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Article 7 [ Fall by 01-12-2010]

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Article 8 [ Expired by 01-12-2010]

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Article 9 [ Expired by 01-12-2010]

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Article 9a [ Expired by 01-12-2010]

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Paragraph 3. Preparations

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Article 10

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  • 2 The limit values referred to in paragraph 1 shall not apply where lower limit values are set out in Part 3 of Annex VI to Regulation (EC) No 2083/2 of the EC Treaty. Either the 1272/2008 or Annex II, Part B, or Annex III, Part B of the preparationsdirective, unless otherwise specified in Annex V to the preparationdirective.


Article 11

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  • 1 The hazards of a preparation resulting from its physico-chemical properties are assessed by determining these properties of the preparation using the method set out in Annex V, part A, to the substances Directive on the basis of which it can be properly classified and labelled in accordance with the criteria set out in Annex VI to the Regulation on substances.

  • 2 The assessment referred to in paragraph 1 may be omitted if:

    • a. No component of that preparation is classified in a category as specified in Article 9.2.3.1, second paragraph, parts (a) to (e) of the Act and, according to the data available to the manufacturer, it is unlikely that such a hazard is present in the preparation;

    • b. in the case of modification of the composition of a preparation of known composition, there is scientific evidence that a new hazard assessment will not lead to a change in the classification;

    • (c) preparations which have been placed on the market in the form of aerosols and which comply with the provisions of Article 9a of this Regulation. Directive No 75 /324/EEC of the Council of 20 May 1975 on the approximation of the laws of the Member States relating to aerosol dispensers (PbEG L 147).

  • 3 In cases where the methods set out in Annex V, Part A, are not suitable for the substances Directive, the alternative calculation methods set out in Part B of Annex I to the preparationsdirective shall be used.

  • 4 The exemption from the application of the methods set out in Annex V, Part A of the substances Directive shall apply to Part A of Annex I to the preparationsdirective.

  • 5 The risks arising from the physico-chemical properties of a preparation covered by the plant protection resources directive are assessed by determining its physico-chemical properties according to which it can be properly identified. shall be classified in accordance with the criteria set out in Annex VI to this Directive. These physico-chemical properties shall be determined by the methods set out in Annex V, Part A, to the substances Directive, unless other internationally recognised methods are acceptable in accordance with the provisions of Annexes II and III. in the case of pesticides Directive


Article 12

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  • 1 The risks of a preparation for health shall be assessed in accordance with one or more of the following procedures:

    • a. by means of a conventional method described in Annex II to the preparationsdirective;

    • b. by the determination of the toxicological properties of the preparation so that it can be appropriately classified according to the criteria set out in Annex VI to the Regulation on substances. These characteristics are determined by the methods set out in Annex V, Part B, to the substances Directive, unless, in the case of a preparation covered by the plant protection products Directive, other internationally recognised methods are acceptable in compliance with the provisions of Annexes II and III to the Plant Protection Products Directive.

  • 2 The methods referred to in paragraph 1 (b) shall be used only, in the case of:

    • a. in accordance with Article 12 of Directive No 86 /609/EEC -of the Council of 24 November 1986 on the approximation of the laws, regulations and administrative provisions of the Member States concerning the protection of animals used for experimental and other scientific purposes (PbEG L 358) is justified or specifically permitted, without prejudice to the provisions of the Plant Protection Products Directive,

    • (b) where the person responsible for placing the preparation on the market can prove scientifically that the toxicological properties of the preparation cannot be correctly determined by the first paragraph, the method referred to, or the results of experiments carried out with animals.

  • 3 When a toxicological property is established with the methods described in paragraph 1 (b) for obtaining new data, the test shall be carried out in accordance with the principles of good laboratory practice such as fixed at Directive No 2004 /10/EC of the European Parliament and of the Council of 11 February 2004 on the approximation of laws, regulations and administrative provisions relating to the application of the principles of good laboratory practice and the supervision of the application for tests on chemical substances (PbEG L 50), as established by Directive No 86 /609/EEC -of the Council of 24 November 1986 on the approximation of the laws, regulations and administrative provisions of the Member States concerning the protection of animals used for experimental and other scientific purposes (PbEG L 358), and in particular Articles 7 and 12 of that Directive.

  • 4 Where a toxicological property has been established using both a method and referred to in paragraph 1 (a) and a method referred to in paragraph 1 (b), the results of the first paragraph, part b, shall be set out in Annex II to the Annex. Methods used for inparts of the preparation.

  • 5 By way of derogation from the fourth paragraph, subject to paragraph 6 and seventh paragraph, only the first paragraph, part a, shall apply in the case of carcinogenic, mutagenic or reproductive toxic effects.

  • 6 A preparation is classified on the basis of effects on humans when, by epidemiological studies, scientifically based case studies as defined in Annex VI to the substances directive or by statistically based experience, Such as the assessment of data from poison centres or occupational diseases, it shall be demonstrated that the toxicological effects on man are different from that based on the application of the methods of the first paragraph.

  • 7 In the classification of the preparation, account is taken of phenomena such as potentiation or antagonism, where it is shown that the toxicological hazard in a conventional assessment is underestimated as a result of these phenomena It's over-treasure.

  • 8 With the methods referred to in paragraph 1 (a) or (b), a new assessment of the risks to health of preparations known to be composed shall be carried out if:

    • a. the manufacturer modifies the original concentration of one or more of the health-hazardous components of the preparation, expressed as a volume or volume, by a greater percentage than the percentage of the content of the preparation Annex II in this arrangement;

    • (b) the manufacturer shall change the composition of the preparation by replacing or adding one or more components which may or may not be dangerous in the sense of Article 9.2.3.1, second paragraph, of the Act .

  • 9 The eighth paragraph shall not apply where:

    • (a) preparations covered by the plant protection resources directive which have been classified according to the method referred to in paragraph 1 (b);

    • b. There is good scientific evidence that a new hazard assessment will not lead to a different classification.


Article 13

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  • 1 The risks of a preparation for the environment shall be assessed in accordance with one or more of the following procedures:

    • a. through the conventional method described in Annex III to the preparationsdirective;

    • b. by the determination of the environmentally hazardous properties of the preparation under which it can be properly classified according to the criteria set out in Annex VI to the Regulation on substances. These characteristics shall be determined by the methods set out in Annex V, Part C, to the Directive unless, in the case of plant protection products, other internationally recognised methods are acceptable according to the provisions of the Directive. Annexes II and III to the Plant Protection Products Directive. Without prejudice to the test requirements of the plant protection products Directive, the conditions for the application of the test methods set out in Part C of Annex III to the preparationsdirective are met.

  • 2 Where an ecotoxic property has been determined by means of one of the methods referred to in paragraph 1 (b), new data shall be collected using tests carried out in accordance with the appropriate tests. laboratory practice of Directive No 2004 /10/EEC of the European Parliament and of the Council of 11 February 2004 on the approximation of laws, regulations and administrative provisions relating to the application of the principles of good laboratory practice and the supervision of the application for tests on chemical substances (PbEG L 50), and the provisions of Directive No 86 /609/EEC -of the Council of 24 November 1986 on the approximation of the laws, regulations and administrative provisions of the Member States concerning the protection of animals used for experimental and other scientific purposes (PbEG L 358).

  • 3 The result of the method referred to in paragraph 1 (b) shall determine the classification of the preparation when the hazards to the environment have been established by both methods referred to in paragraph 1.

  • 4 The methods referred to in paragraph 1 (a) or (b) shall be subject to a new assessment of the risks to the environment of preparations whose composition is known, if:

    • a. the manufacturer modifies the original concentration of one or more environmental hazardous components of the preparation, expressed as a volume or volume, by a greater percentage than the percentage recorded in the weight of the product concerned. Annex II in this arrangement;

    • (b) the manufacturer shall change the composition of the preparation by replacing or adding one or more components which may or may not be dangerous in the sense of Article 9.2.3.1, second paragraph, of the Act .

  • 5 The fourth paragraph shall not apply where:

    • (a) preparations covered by the plant protection resources directive which have been classified according to the method referred to in paragraph 1 (b);

    • b. There is good scientific evidence that a new hazard assessment will not lead to a different classification.


Article 14

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  • 1 Without prejudice to the provisions of Article 1a, first paragraph, of the Decision The following particulars shall be clearly marked and indelibly marked on each package of a preparation:

    • a. The name or trade name of the preparation;

    • (b) the name and full address, including telephone number, of the person responsible for placing the preparation on the market and established in the Community, whether or not it is the manufacturer, the importer or the distributor;

    • (c) the chemical name of the substance (s) present in the preparation, as follows:

      • 1 °. for preparations which, in accordance with Article 12 (1), + , T or Xn are classified, only account is taken of the T + -, T-or Xn-substances present in a concentration equal to or greater than their respective lowest limit value (the Xn limit) as set out in Part 3 of Annex VI to Regulation (EC) No 2383/2 of Regulation (EC) No 2028/18 (2). 1272/2008, or, in the absence thereof, in Annex II, Part B to the preparationsdirective;

      • 2 °. for preparations classified as C in accordance with Article 12, only the C-substances present in a concentration equal to or greater than their lowest limit values the (the Xi limit) as established shall be taken into account. In Part 3 of Annex VI to Regulation (EC) No 1272/2008 or, in the absence thereof, in Annex II, Part B, to the preparationsdirective;

      • 3 °. on the label, the name of the substance or substances on the basis of which the preparation is classified in one or more of the following hazard categories is given:

        • -carcinogenic, category 1, 2 or 3,

        • -mutagenic, category 1, 2 or 3,

        • -toxic for reproduction, category 1, 2 or 3,

        • -very toxic, toxic or harmful due to non-lethal effects after one exposure,

        • -toxic or harmful due to severe effects after repeated or long-term exposure,

        • -sensitising;

      • 4 °. in the form of one of the parts listed in Part 3 of Annex VI to Regulation (EC) The nomenclature used in an internationally recognised chemical nomenclature shall be used in accordance with the terms of the Regulation (s) of Regulation (EC) No 1272/2008 or, if the substance is not

    • d. The nominal mass or volume of preparations when they are preparations which are presented to the general public.

  • 3 By way of derogation from paragraph 1 (c), first to third subsubparagraphs, it shall be sufficient to indicate a maximum of four chemical names for the identification of the substances which are principally responsible for packaging, for the major health hazards which have led to the classification and the choice of the corresponding standard phrases for the identification of particular hazards. In some cases more than four chemical names may be necessary.

  • 4 The symbols of danger, to the extent laid down in the Directive, and the indications of the hazards associated with the use of that preparation which must be indicated on the packaging, are in accordance with the instructions of the Directive. Annex II and Annex VI to the substances Directive shall be affixed in accordance with the results of the hazard assessment described in Annexes I, II and III to the Directive.

  • 5 By way of derogation from the fourth paragraph, where more than one danger symbol is assigned to a preparation:

    • a. The affixing to the packaging of the symbols C and X shall not be compulsory where the obligation exists to affea the symbol 'T' to the packaging;

    • (b) the affixing of the symbol 'X' on the packaging does not require the affixing of the symbol 'C', unless otherwise provided for in Part 3 of Annex VI to Regulation (EC) No 2383/2 of the EC Treaty; 1272/2008;

    • c. The affixing of the symbols F and O to the packaging shall not be compulsory where the obligation exists to affer the symbol 'E' on the packaging;

    • (d) The affixing of the symbol 'Xi' on the packaging shall not be compulsory where the obligation exists on the packaging to be affixed to the packaging.

  • 6 The symbols are printed in black on an orange-yellow background.

  • 7 The risk phrases indicating the particular hazards shall be in accordance with the instructions set out in Annex III and Annex VI to the substances Directive and shall be applied in accordance with the results of the requirements set out in Annexes I, II and III to the Annex to this Directive. the preparationsdirective described the hazard assessment. The packaging shall be sufficient to indicate a maximum of six hazard phrases indicating the hazards, provided that these warning phrases are not related to pesticides. The combination phrases set out in Annex III to the substances Directive shall be counted as one sentence each time.

  • 8 If a preparation belongs to more than one hazard category at the same time, the standard phrases on the pack include all major hazards associated with the preparation. In this case, the limitation shall not apply to a maximum of six warning phrases referred to in paragraph 7 for the purpose of indicating the hazards.

  • 9 The indication on the packaging of the risk phrases 'extremely flammable' or 'highly flammable' may be omitted from a hazard designation made in accordance with the fourth and fifth paragraphs.

  • 10 Safety recommendations on the packaging are in accordance with the instructions set out in Annex IV and with Annex VI to the Directive on substances and shall be made according to the results of the Annexes I, II and III to the Directive. Preparationsdirective described the hazard assessment. The packaging shall be sufficient to indicate a maximum of six phrases for the formulation of the most appropriate security-based auctions, provided that such safety recommendations are not related to pesticides. The combination phrases set out in Annex IV to the substances Directive are counted as one sentence each time.

  • 11 Where, in practical terms, it is not possible to make the safety recommendations for use of the preparation on the label or on the packaging itself, they shall be attached to the packaging.

  • 12 Where a package may not contain more than 125 ml, the following shall be required:

    • a. In the case of preparations which are classified as highly flammable, oxidizing, irritant, with the exception of preparations with a warning phrase R41, or as an environmental hazard and to which the N symbol has been assigned, the risk phrases and the warning phrases security recommendations not to be stated;

    • b. In the case of preparations which are classified as flammable or environmentally hazardous and to which the N symbol has not been assigned, the safety recommendations shall not be indicated.

  • 13 Without prejudice to the first up to and including twelfth members, preparations classified in a category as referred to in Article 9.2.3.1, second paragraph, of the Act , placed on the market only if the marking on the packaging complies with the provisions of Annex V, Part A and B to the preparation directive relating to the preparation concerned.

  • 14 Without prejudice to paragraph 1 (a) and (b), preparations not classified in a category as referred to in paragraph 1 shall be classified in Article 9.2.3.1, second paragraph, of the Act but which may nevertheless pose a specific hazard, placed on the market only if the marking on the packaging complies with the provisions of Annex V, Part B and C to the preparation directive relating to the preparation concerned.


Article 15

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  • (1) If the person responsible for placing a preparation on the market can prove that publication on the label or safety data sheet of the chemical identity of a substance present in that preparation is published, which is solely Classified as:

  • 2 The first paragraph shall not apply to preparations containing substances for which an exposure limit has been established.

  • 3 Where a case referred to in the first paragraph arises and the preparation is placed on the market for the first time in a Member State of the European Union or a State party to the Agreement on the European Economic Area, The person responsible for placing on the market of a preparation shall address the request, in accordance with Annex VI to the Directive, to the Minister for Health, Welfare and Sport. The request is submitted to the Dutch Food and Warenauthority.


Article 15a

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  • 1 The label or packaging shall only bear the particulars required under the preparation Directive and any additional health or safety recommendations.

  • 2 If the Article 14 It shall be affixed firmly to one or more sides of the package so that these particulars can be read horizontally when the packaging has been put down in the usual manner.

  • 3 The dimensions of the label and the presentation and the format of the conformity Article 14 information required on the label shall comply with Annex VI to the Directive.

  • 4 The colour and appearance of the label and the packaging shall be chosen so as to clearly set the symbol and the background to it.

  • 6 In the case of packaging as referred to in paragraph 5, indications shall be given, in addition to the particulars provided for in that paragraph, in accordance with the provisions of Annex VI to the Directive, if the special nature of the package so provides necessary.


Article 15b

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  • 1 The Articles 9.2.3.1 to 9.2.3.4 of the Act and the Articles 1a and 5 of the Decision shall apply mutatis mutandis to preparations for preparations intended for export to a country other than a Member State of the European Union or a State party to the Agreement on the European Economic Area, without prejudice to the specific specific and relevant rules laid down by the country to which the relevant preparations are intended, on the packaging and marking.

  • 2 By way of derogation from paragraph 1, the conditions laid down by the importing country for the designation of the preparation shall apply if they provide the same guarantee as regards the protection of health, safety and the environment as a result of the application of the preparation of the preparation of the preparation of the preparation of the preparation of the preparation of the the requirements relating to or pursuant to the requirements of the Articles 9.2.3.1 to 9.2.3.4 of the Act .

  • 3 The particulars given on the packaging under the first paragraph shall be drawn up in the language or in one or more of the main languages of the country or territory in which the preparation is intended, if this is practicable.


Article 15c

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  • 1 Without prejudice to the provisions of the Articles 14 , 15a and 15b shall be clearly legible and indelibly marked on the label for pesticides:

    • a. The College for the authorisation of plant protection products and biocidal products as referred to in Article 3 of the Plant Protection Products Act and biocidal products the authorisation or registration number granted to the control agent;

    • b. The nature of the preparation, such as liquid concentrate, granules, powder, solid substance, spray powder or emulsifiable concentrate;

    • c. Applications for which the pesticide is authorised, such as wood preservative, disinfection, surface biocide, fouled, insecticide, growth regulator or herbicide;

    • d. For each use specified in the conditions of admission, the instructions for use and the dose expressed in metric units;

    • e. guidance on the provision of first aid;

    • f. the sentence 'Read the enclosed instructions for use', if a package leaflet is attached;

    • g. instructions for safe removal of the material for the use of the material and its packaging;

    • h. The batch number of the preparation; and where applicable:

    • i. categories of users authorised to use the pesticide;

    • j. in Annex III cca logo included in this arrangement, which provides for the separation and separation of products which are small chemical waste at the waste stage, in so far as they are intended to be used as a means of control for domestic products Use.

  • 2 The first paragraph, part j, shall not apply:

    • a. Pesticides consisting exclusively of micro-organisms or viruses;

    • b. on pesticides in the European Waste List Scheme have not been designated as hazardous waste;

    • (c) Where the packaging is marked with an indication to be given in a Member State of the European Union of the public in respect of the separation and separation of plant protection products containing small chemical substances at the waste stage, waste.

  • 3 Without prejudice to other information obligations, samples, models or designs of the packaging, labels and attachment agents shall be provided to the College for the authorisation of plant protection products and biocidal products as referred to in Article 3 of the Plant Protection Products Act and biocidal products in the context of the authorisation or registration.

  • The packaging of a pesticide shall be sealed in such a way that it cannot be opened without damage to the seal. This does not apply to those provided for by way of derogation from the prohibition in question. Article 2, first paragraph, of the Pesticide Decision , held or kept in stock or delivered in a package other than that in which they were first put into circulation here.


Article 15d

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  • 1 Without prejudice to the provisions of the Articles 14 , 15a , 15b and 15c shall be:

    • (a) clearly legible and indelibly marked on the label of biocidal products:

      • 1 °. the nature of each active substance and its concentration in metric units;

      • 2. details of possible direct or indirect adverse reactions;

      • 3 °. where applicable, a prohibition on the re-use of the packaging;

      • 4 °. the batch indication and the due date under normal storage conditions;

      • 5 °. time expiring before the action of the biocidal product enters into force, the period to be taken into account between two consecutive treatments with the biocidal product or between a treatment and the next use of the treated product or the the next person or animal of the area where the biocidal product has been used, including details of the means of contamination and measures and how long the spaces in question must be ventilated; details of the Adequate cleaning of equipment; details of precautions taken during the period use, storage and transport, such as protective, individual clothing and equipment, fire safety measures, decks of furniture, food and feed disposal and evidence to prevent exposure of animals; and where of application:

      • 6 °. information on the environmental hazards, in particular with regard to the protection of non-target organisms and the prevention of water pollution;

    • b. are labelled microbiological biocides in accordance with regulatory compliance with or under the Labor condition law .

  • 2 By way of derogation from the first paragraph, the Article 15c, first paragraph, parts b, d, e, g and h The information referred to in paragraph 1 (a), second to sixth, shall be clearly and indelibly marked elsewhere on the packaging or on a package leaflet accompanying the pack.

  • 3 Biocidal products which may be confused with food, drink or feed shall be packed in such a way that the possibility of confusion is as low as possible.

  • In the case of biocidal products available to the general public and confused with food, drink or feed, constituents shall be added to counteract their consumption.


Article 15th

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  • a. The label shall state clearly and indelibly on the label for plant protection products 'follow the instructions for use in order to prevent danger to man and the environment';

  • (b) on the packaging for plant protection products, clearly legibly and indelibly:

    • 1 °. the content of each active substance;

    • 2 °. the net quantity of the plant protection product, expressed in statutory units of measurement;

    • 3 ° where applicable, a given enabling the preparation of the preparation of the preparation;

    • 4. the nature of any particular hazards to humans, animals or the environment in the form of standard formulations, the wording of which is an appropriate choice for the species listed in Annex IV to the Plant Protection Products Directive. standard formulations;

    • 5 °. the safety precautions for the protection of man, animals or the environment in the form of standard formulations, for which formulation an appropriate choice is made from the Annex V to the Plant Protection Products Directive; standard formulations;

    • 6 °. the use for which the plant protection product is authorised and any agricultural, plant-health and environmental conditions under which the product may be used or not be used;

    • 7 °. if necessary, for each use the time limit for the safety to be established between an application and sowing or planting of the crop to be protected, the sowing or planting of subsequent crops, human and animal access, harvesting, consumption or consumption;

    • 8 °. details of possible phytotoxicity, susceptibility of certain varieties and all other direct or indirect harmful side effects on plants or plant products, as well as the periods to be observed between an application and sowing or planting of the relevant crop, or any subsequent crop; and

    • 9 °. the final use date under normal storage conditions if the product is tenable for less than two years.

  • c. if the package is so small that it is not reasonable to provide all the prescribed terms and particulars, use either of a label attached to the packaging in an appropriate manner or of a label of a kind used in the package. included in the package enclosed in the package leaflet, except that:

    • 1 °. on the packaging, at least: the name of the plant protection product, the approval number and the batch number, the symbol of danger if required and, where necessary, the logo logo and a reference to the package leaflet or the label;

    • 2 °, the package leaflet or the label shall state all the prescribed particulars and particulars, except for the batch number.

  • d. may indicate on the label that the plant protection product may be used when bees or other non-target species are active or crops or weeds are in bloom, or similar indications to bees or other non-target species. shall protect, where the authorisation expressly refers to use during the periods when bees or other specified organisms are present and the means of a minimum risk posed by these organisms.


Article 15f

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Dangerous preparations listed in Annex VII to the Directive which are classified in a category as referred to in the Annex Article 9.2.3.1, second paragraph, of the Act , those in the form in which they are placed on the market do not pose hazards from physico-chemical properties, nor health or environmental hazards, are the Articles 9.2.3.3 and 9.2.3.4 of the Act , Article 1a of the Decision of Packaging and Indication of Environmental Hazardous Substances and Preparations , the Articles 3 , 4 and 5 of the WarenwetDecree safe packaging of household chemicals and the Articles 14 , 15a , 15c and 15th , not applicable.


Article 15g

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The person responsible for the placing on the market of a substance or preparation shall keep the information referred to in Article 6d, first paragraph, of the Decision at the disposal of the Netherlands Food and Warenes Authority, the Labour Inspectorate and the Inspectorate of Environmental Hygiene.


Article 15h

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The National Poisonings Information Centre is responsible for the performance of the task referred to in Article 45 (1) of Regulation (EC) No 148/ (2). 1272/2008.


Paragraph 4. Final provisions

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Article 16

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This scheme is based on: Article 1a, second and third paragraphs , 6, second paragraph, of the Decision and Article 9.3a.1 of the Act .


Article 17

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The Declaration Of Delivery Of Dangerous Substances (Stcrt. 1980, 64) is hereby repealed.


Article 18

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The Declaration Of Delivery Of Dangerous Preparations (Stcrt. 1980, 64) is hereby repealed.


Article 19

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  • 2 An amendment to Annexes II, III, IV, V or VI to the Directive shall enter into force for the purpose of applying the related articles from the day on which the relevant amending Directive is to be implemented at the latest. given.

  • 3 An amendment to Annex I, II, III, IV, V, VI or VII to the preparationdirective shall enter into force for the purpose of applying this scheme from the date on which the relevant amending Directive is to be implemented, unless Ministerial arrangement which is published in the Official Journal of the European Union and published in the Official Gazette is another date.

  • 4 In the case of a ministerial arrangement, parts of a change which has entered into force as referred to in paragraph 3 may be left out of use for the categories of preparations to be notified under that arrangement until a time to be specified.

  • 5 It can be quoted as 'Detailed Packaging and Indication of Environmental Hazardous Substances and Preparations'.

Rijswijk, 27 January 1988

The

State Secretary

of Welfare, Health and Culture,

D. J. D. Dees

The

Minister

of Housing, Spatial Planning and the Environment,

E. H. T. M. Nipples

The

State Secretary

of Social Affairs and Employment,

L. de Graaf


Annex I

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Category in which the dangerous substance is classified

Limit values for

Gaseous preparations

(volume percent)

Other preparations

(% by weight)

Very toxic

≥ 0, 02

≥ 0, 1

Toxic

≥ 0, 02

≥ 0, 1

Carcinogenic

Category 1 or 2

≥ 0, 02

≥ 0, 1

Mutagenic

Category 1 or 2

≥ 0, 02

≥ 0, 1

Toxic for reproduction

Category 1 or 2

≥ 0, 02

≥ 0, 1

Harmful

≥ 0, 2

≥ 1

Corrosive

≥ 0, 02

≥ 1

Irritating

≥ 0, 2

≥ 1

Sensitising

≥ 0, 2

≥ 1

Carcinogenic

Category 3

≥ 0, 2

≥ 1

Mutagenic

Category 3

≥ 0, 2

≥ 1

Toxic for reproduction

Category 3

≥ 0, 2

≥ 1

Hazardous to the environment N

≥ 0, 1

Hazardous to the environment ozone

≥ 0, 1

≥ 0, 1

Hazardous to the environment

≥ 1


Annex II

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Interval of the original concentration of the component

Permitted variation of the original concentration of the component

≤ 2, 5%

± 30%

> 2, 5 ≤ 10%

± 20%

> 10 ≤ 25%

± 10%

> 25 ≤ 100%

± 5%


Annex III

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