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Document 32011D0785

    2011/785/EU: Commission Implementing Decision of 28 November 2011 amending Decision 2008/911/EC establishing a list of herbal substances, preparations and combinations thereof for use in traditional herbal medicinal products (notified under document C(2011) 7382) Text with EEA relevance

    OJ L 319, 02/12/2011, p. 102–105 (BG, ES, CS, DA, DE, ET, EL, EN, FR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

    ⏵This document has been published in a special edition(s) (HR)

    Legal status of the document In force

    ELI: http://data.europa.eu/eli/dec_impl/2011/785/oj

    Date of document:
    28/11/2011
    Date of effect:
    29/11/2011; Takes effect Date notif.
    Date of notification:
    29/11/2011
    Date of end of validity:
    No end date
    Author:
    European Commission
    Responsible body:
    Directorate-General for Health and Food Safety
    Form:
    Implementing decision
    Addressee:
    The twenty-seven Member States: Belgium, Bulgaria, Czech Republic, Denmark, Germany, Estonia, Ireland, Greece, Spain, France, Italy, Cyprus, Latvia, Lithuania, Luxembourg, Hungary, Malta, Netherlands, Austria, Poland, Portugal, Romania, Slovenia, Slovakia, Finland, Sweden, United Kingdom
    Additional information:
    EEA relevance
    Treaty:
    Treaty on the Functioning of the European Union , Treaty on European Union
    Legal basis:
    Link
    Link
    Link
    Select all documents mentioning this document
    Modifies:
    Relation Act Comment Subdivision concerned From To
    Modifies 32008D0911 Amendment annex I
    Modifies 32008D0911 Amendment annex II
    Link

    2.12.2011   

    EN

    Official Journal of the European Union

    L 319/102

    COMMISSION IMPLEMENTING DECISION

    of 28 November 2011

    amending Decision 2008/911/EC establishing a list of herbal substances, preparations and combinations thereof for use in traditional herbal medicinal products

    (notified under document C(2011) 7382)

    (Text with EEA relevance)

    (2011/785/EU)

    THE EUROPEAN COMMISSION,

    Having regard to the Treaty on European Union and the Treaty on the Functioning of the European Union,

    Having regard to Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use (1), and in particular Article 16f thereof,

    Having regard to the opinion of the European Medicines Agency, formulated on 15 July 2010 by the Committee for Herbal Medicinal Products,

    Whereas:

    (1)

    Hamamelis virginiana L. can be considered as a herbal substance, a herbal preparation or a combination thereof within the meaning of Directive 2001/83/EC and complies with the requirements set out in that Directive.

    (2)

    It is therefore appropriate to include Hamamelis virginiana L. in the list of herbal substances, preparations and combinations thereof for use in traditional herbal medicinal products established by Commission Decision 2008/911/EC (2).

    (3)

    Decision 2008/911/EC should therefore be amended accordingly.

    (4)

    The measures provided for in this Decision are in accordance with the opinion of the Standing Committee on Medicinal Products for Human Use,

    HAS ADOPTED THIS DECISION:

    Article 1

    Annexes I and II of Decision 2008/911/EC are amended in accordance with the Annex to this Decision.

    Article 2

    This Decision is addressed to the Member States.

    Done at Brussels, 28 November 2011.

    For the Commission

    John DALLI

    Member of the Commission

    (1)   OJ L 311, 28.11.2001, p. 67.

    (2)   OJ L 328, 6.12.2008, p. 42.

    ANNEX

    Annexes I and II to Decision 2008/911/EC are amended as follows:

    1.

    in Annex I, the following substance is inserted after Foeniculum vulgare Miller subsp. vulgare var. dulce (Miller) Thellung (sweet fennel fruit):

    ‘ Hamamelis virginiana L., folium et cortex aut ramunculus destillatum ’;

    2.

    in Annex II, the following is inserted after the entry relating to Foeniculum vulgare Miller subsp. vulgare var. dulce (Miller) Thellung, fructus:

    ‘ COMMUNITY LIST ENTRY ON HAMAMELIS VIRGINIANA L., FOLIUM ET CORTEX AUT RAMUNCULUS DESTILLATUM

    Scientific name of the plant

    Hamamelis virginiana L.

    Botanical family

    Hamamelidaceae

    Herbal preparation(s)

    1.

    Distillate prepared from fresh leaves and bark (1:1.12 – 2.08; extraction solvent ethanol 6 % m/m)

    2.

    Distillate prepared from dried twigs (1:2; extraction solvent ethanol 14-15 %) (*1)

    European pharmacopoeia monograph reference

    Not applicable

    Indication(s)

    Indication (a)

    Traditional herbal medicinal product for relief of minor skin inflammation and dryness of the skin.

    Indication (b)

    Traditional herbal medicinal product to be used for the temporary relief of eye discomfort due to dryness of the eye or to exposure to wind or sun.

    The product is a traditional herbal medicinal product for use in specified indications exclusively based upon long-standing use.

    Type of tradition

    European

    Specified strength

    Please see ‘Specified posology’.

    Specified posology

    Children over six years of age, adolescents, adults and elderly

    Indication (a)

    Distillate in a strength corresponding to 5-30 % in semi-solid preparations, several times daily.

    The use in children under six years of age is not recommended (see section ‘Special warnings and precautions for use’).

    Adolescents, adults and elderly

    Indication (b)

    Eye drops (*2) Distillate (2) diluted (1:10), 2 drops/each eye, 3-6 times daily.

    The use in children under 12 years of age is not recommended (see section ‘Special warnings and precautions for use’).

    Route of administration

     

    Cutaneous use.

     

    Ocular use.

    Duration of use or any restrictions on the duration of use

    Children over six years of age, adolescents, adults and elderly

    Indication (a)

    If the symptoms persist longer than two weeks during the use of the medicinal product, a doctor or a qualified healthcare practitioner should be consulted.

    Adolescents, adults and elderly

    Indication (b)

    The recommended duration of use is four days. If the symptoms persist longer than two days during the use of the medicinal product, a doctor or a qualified healthcare practitioner should be consulted.

    Any other information necessary for the safe use

    Contraindications

    Hypersensitivity to the active substance.

    Special warnings and precautions for use

    Indication (a)

    The use in children under six years of age has not been established due to lack of adequate data.

    Indication (b)

    If eye pain, changes in vision, continued redness, or irritation of the eye is experienced, or if the condition worsens or persists for more than 48 hours during the use of the medicinal product, a doctor or a qualified healthcare practitioner should be consulted.

    The use in children under 12 years of age has not been established due to lack of adequate data.

    For extracts containing ethanol, the appropriate labelling for ethanol, taken from the ‘Guideline on excipients in the label and package leaflet of medicinal products for human use’, must be included.

    Interactions with other medicinal products and other forms of interaction

    None reported.

    Pregnancy and lactation

    Safety during pregnancy and lactation has not been established. In the absence of sufficient data, the use during pregnancy and lactation is not recommended.

    Effects on ability to drive and use machines

    No studies on the effect on the ability to drive and use machines have been performed.

    Undesirable effects

    Indication (a)

    Allergic contact dermatitis may occur in sensitive patients. The frequency is not known.

    Indication (b)

    Conjunctivitis cases have been reported. The frequency is not known.

    If other adverse reactions not mentioned above occur, a doctor or a qualified healthcare practitioner should be consulted.

    Overdose

    No case of overdose has been reported.

    Pharmaceutical particulars [if necessary]

    Not applicable.

    Pharmacological effects or efficacy plausible on the basis of long-standing use and experience [if necessary for the safe use of the product]

    Not applicable.

    (*1)  According to USP (USP-31- NF 26, 2008 Vol 3:3526)."

    (*2)  The medicinal product complies with the Ph. Eur. monograph on eye preparations (01/2008:1163).’."

    (*1)  According to USP (USP-31- NF 26, 2008 Vol 3:3526).

    (*2)  The medicinal product complies with the Ph. Eur. monograph on eye preparations (01/2008:1163).’.’

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