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Commission Regulation (EEC) No 3600/92 ANNEX I

Commission Regulation (EEC) No 3600/92 ANNEX I

ANNEX ISupplementary provisions

LIST OF SUBSTANCES COVERED BY THE FIRST STAGE OF THE WORK PROGRAMME PROVIDED FOR IN ARTICLE 8 (2) OF DIRECTIVE 91/414/EEC Name 1. Acephate 2. Metamidophos 3. Aldicarb 4. Amitraz 5. Azinphos-ethyl 6. Azinphos-methyl 7. Carbendazim 8. Benomyl 9. Thiophanate-methyl 10. Chlorpyriphos 11. Chlorpyriphos-methyl 12. Cyfluthrin 13. Beta-cyfluthrin 14. Cyhalothrin 15. Lambda-cyhalothrin 16. Cypermethrin 17. Alpha-cypermethrin 18. DNOC 19. Deltamethrin 20. Dinoterb 21. Endosulfan 22. Fenthion 23. Fenvalerate 24. Esfenvalerate 25. Lindane 26. Parathion 27. Parathion-methyl 28. Permethrin 29. Benalaxyl 30. Metalaxyl 31. Chlorothalonil 32. Dinocap 33. Fenarimol 34. Fentin acetate 35. Fentin hydroxide 36. Flusilazole 37. Imazalil 38. Mancozeb 39. Maneb 40. Zineb 41. Metiram 42. Propineb 43. Thiram 44. Ferbam 45. Ziram 46. Propiconazole 47. Pyrazophos 48. Quintozene 49. Thiabendazole 50. Vinclozolin 51. Procymidone 52. Iprodione 53. Chlozolinate 54. Chlorpropham 55. Propham 56. Daminozide 57. Maleic hydrazide 58. Tecnazene 59. Alachlor 60. Amitrole (Aminotriazole) 61. Atrazine 62. Simazine 63. Bentazone 64. Chlorotoluron 65. 2,4-D 66. 2,4-DB 67. Ethofumesate 68. Fluroxypyr 69. Glyphosate 70. Ioxynil 71. Bromoxynil 72. Isoproturon 73. MCPA 74. MCPB 75. Mecoprop 76. Mecoprop-P 77. Metsulfuron 78. Tifensulfuron 79. Triasulfuron 80. Molinate 81. Monolinuron 82. Linuron 83. Paraquat 84. Diquat 85. Pendimethalin 86. Desmedipham 87. Phenmedipham 88. Propyzamide 89. Pyridate 90. Warfarin ANNEX II MODEL Notification of an active substance according to Article 4 (1) of Regulation (EEC) No 3600/92 1. Identification data on the notifier 1.1 Manufacturer of the active substance (name, address, including location of plant): 1.2 Notifying company (name, address, etc.) (if different from 1.1): 1.2.a. Acting as: - sole representative designated by the manufacturer, - importer not designated as sole representative of the manufacturer. 1.3 Name of the (physical) person responsible for the notification and further engagements resulting from Regulation (EEC) No 3600/92. 1.3.1. Address for correspondence: 1.3.2. (a) Telephone No: (b) Telex No: (c) Telefax No: 1.3.3. (a) Contact: (b) Alternative: 2. Information to facilitate identification 2.1 Common name proposed or ISO-accepted, and synonyms, specifying, where relevant, any salts or esters produced by the manufacturer. 2.2 Chemical name (IUPAC nomenclature). 2.3 Manufacturer's development code number(s). 2.4 CAS, CIPAC and EEC numbers (if available). 2.5 Empirical and structural formula, molecular mass. 2.6 Specification of purity of the active substance in g/kg or g/l as appropriate. 2.7 Identity of isomers, impurities and additives (e.g. stabilizers), together with the structural formula and the possible range expressed in g/kg or g/l. 3. Information on use conditions to be covered by the inclusion in Annex I and supported by the applicant 3.1 Function, e.g. fungicide, herbicide, insecticide, repellant, growth regulator. 3.2 Field of use envisaged, e.g. field, glasshouse, food or feed storage, home garden. 3.3 Any specific health, agricultural, plant health or environmental conditions under which the active substance may or should not be used. 3.4 Harmful organisms controlled and crops or products protected or treated. 4. Information on authorized uses known to the notifier 4.1 Countries where there is registration (EC). 4.2 Contries where there is registration (non EC). 4.3 Registered uses in EC, including all relevant conditions. 4.4 Formulations Name, type (GIFAP/FAO code) and content of active substance (in g/kg or g/l). 5. Undertaking to submit dossier The notification confirms that the above information is honest and correct. He agrees to submit to the competent authorities of the designated reporting Member State the dossiers as set out in Article 6 of Regulation (EEC) No 3600/92 within a period of 12 months of the Commission decision provided for in Article 5 (4) of this Regulation. Whenever this decision mentions several notifiers for this active substance, the notifier will undertake all reasonable efforts to present a single dossier collectively with the other notifiers. Signature (of the person competent to act for the company mentioned under 1.1).

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Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗ · Data as of 2026-07-04

CitationANNEX I of Commission Regulation (EEC) No 3600/92 (LawPlayer, data as of 2026-07-04)

© European Union, https://eur-lex.europa.eu, 1998-2026. Reuse authorised under Commission Decision 2011/833/EU, provided the source is acknowledged.

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