Community herbal monograph on Rosa gallica L., Rosa centifolia L., Rosa damascena Mill., flos



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1 July 2014 EMA/HMPC/137299/2013 Committee on Herbal Medicinal Products (HMPC) Community herbal monograph on Rosa gallica L., Rosa centifolia L., Rosa damascena Mill., flos Final Discussion in Working Party on Community monographs and Community list (MLWP) May 2013 July 2013 Adoption by Committee on Herbal Medicinal Products (HMPC) for release for consultation 17 September 2013 End of consultation (deadline for comments). 15 April 2014 Rediscussion in Working Party on Community monographs and Community list (MLWP) 7 May 2014 Adoption by Committee on Herbal Medicinal Products (HMPC) 1 July 2014 Keywords Herbal medicinal products; HMPC; Community herbal monographs; traditional use; Rosa gallica L., Rosa centifolia L., Rosa damascena Mill., flos; Rosae flos; Rose flower BG (bulgarski): Маслодайна роза, цвят CS (čeština): růžový květ DA (dansk): Rosenblomst DE (Deutsch): Rosenblütenblätter EL (elliniká): Ρόδου άνθος EN (English): Rose flower ES (español): Rosa, flor de ET (eesti keel): kibuvitsaõis FI (suomi): ruusu, kukka FR (français): Rose pâle, rose de Provins, rose de Damas HR (hrvatski): ružin cvijet HU (magyar): Rózsavirág IT (italiano): Rosa fiore LT (lietuvių kalba): Rožių žiedai LV (latviešu valoda): Rožu ziedi MT (Malti): Fjura tal-ward NL (Nederlands): Roos, bloem PL (polski): Kwiat róży PT (português): Rosa, flor RO (română): SK (slovenčina): Kvet ruže SL (slovenščina): cvet vrtnice SV (svenska): Rosenblad IS (íslenska): NO (norsk): Roseblomst 30 Churchill Place Canary Wharf London E14 5EU United Kingdom Telephone +44 (0)20 3660 6000 Facsimile +44 (0)20 3660 5520 Send a question via our website www.ema.europa.eu/contact An agency of the European Union European Medicines Agency, 2014. Reproduction is authorised provided the source is acknowledged.

Community herbal monograph on Rosa gallica L., Rosa centifolia L., Rosa damascena Mill., flos 1. Name of the medicinal product To be specified for the individual finished product. 2. Qualitative and quantitative composition 1, 2 With regard to the registration application of Article 16d(1) of Directive 2001/83/EC as amended Rosa gallica L., Rosa centifolia L., Rosa damascena Mill., flos (Rose flower) i) Herbal substance Dried petals ii) Herbal preparations Comminuted herbal substance 3. Pharmaceutical form Herbal substance or comminuted herbal substance for infusion preparation for oromucosal or cutaneous use. The pharmaceutical form should be described by full standard term. 4. Clinical particulars 4.1. Therapeutic indications Indication 1) Traditional herbal medicinal product used for mild inflammations of the oral and pharyngeal mucosa. 1 The material complies with the monograph in the Ph. Fr. XI edition (Rose pâle 1989; Rose rouge 1989). 2 The declaration of the active substance(s) for an individual finished product should be in accordance with relevant herbal quality guidance. EMA/HMPC/137299/2013 Page 2/6

Indication 2) Traditional herbal medicinal product used for relief of minor skin inflammation. The product is a traditional herbal medicinal product for use in specified indications exclusively based upon long-standing use. 4.2. Posology and method of administration 3 Posology Indication 1) Adolescents, adults and elderly Single dose Herbal substance or comminuted herbal substance for infusion preparation for oromucosal use: 1 2 g of the herbal substance or comminuted herbal substance in 200 ml of boiling water As a mouth rinse, up to 3 times daily. The use in children under 12 years of age is not recommended (see section 4.4 Special warnings and precautions for use ). Indication 2) Adolescents, adults and elderly Single dose Herbal substance or comminuted herbal substance for infusion preparation for cutaneous use: 1 2 g of the herbal substance or comminuted herbal substance in 200 ml of boiling water Apply on the affected area, up to 3 times daily, in the form of a wet, impregnated dressing. The use in children under 12 years of age is not recommended (see section 4.4 Special warnings and precautions for use ). 3 For guidance on herbal substance/herbal preparation administered as herbal tea or as infusion/decoction/macerate preparation, please refer to the HMPC Glossary on herbal teas (EMA/HMPC/5829/2010 Rev.1). EMA/HMPC/137299/2013 Page 3/6

Duration of use Indications 1) and 2) If the symptoms persist longer than 1 week during the use of the medicinal product, a doctor or a qualified health care practitioner should be consulted. Method of administration Cutaneous use. Oromucosal use. 4.3. Contraindications Hypersensitivity to the active substance. 4.4. Special warnings and precautions for use Indications 1) and 2) The use in children under 12 years of age has not been established due to lack of adequate. 4.5. Interactions with other medicinal products and other forms of interaction None reported. 4.6. Fertility, pregnancy and lactation No fertility data available. Safety during pregnancy and lactation has not been established. In the absence of sufficient data, the use during pregnancy and lactation is not recommended. EMA/HMPC/137299/2013 Page 4/6

4.7. Effects on ability to drive and use machines No studies on the effect on the ability to drive and use machines have been performed. 4.8. Undesirable effects None known. If adverse reactions occur, a doctor or a qualified health care practitioner should be consulted. 4.9. Overdose No case of overdose has been reported. 5. Pharmacological properties 5.1. Pharmacodynamic properties Not required as per Article 16c(1)(a)(iii) of Directive 2001/83/EC as amended. 5.2. Pharmacokinetic properties Not required as per Article 16c(1)(a)(iii) of Directive 2001/83/EC as amended. 5.3. Preclinical safety data Not required as per Article 16c(1)(a)(iii) of Directive 2001/83/EC as amended, unless necessary for the safe use of the product. Tests on genotoxicity, reproductive toxicity and carcinogenicity have not been performed. EMA/HMPC/137299/2013 Page 5/6

6. Pharmaceutical particulars Not applicable. 7. Date of compilation/last revision 1 July 2014 EMA/HMPC/137299/2013 Page 6/6