Gnc Live Well Horsetail Capsules
Out of date information, search anotherSUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Holland & Barrett Horsetail Capsules GNC Live Well Horsetail Capsules Lifecycle Horsetail Capsules Nature’s Garden Horsetail Capsules Nature’s Bounty Horsetail Capsules
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each hard capsule contains 160mg of extract (as dry extract) from Horsetail herb (Equisetum arvense L.) (equivalent to 640mg - 960mg of Horsetail herb). Extraction solvent: Water
For full list of excipients, see section 6.1
3 PHARMACEUTICAL FORM
Capsule, hard
Two piece clear hard capsules with light brown fill.
4 CLINICAL PARTICULARS
4.1 Therapeutic indications
A traditional herbal medicinal product used to increase the amount of urine for the purpose of flushing the urinary tract to assist in minor urinary complaints. This is based on traditional use only.
Posology and method of administration
4.2
For oral use only.
Adults and the elderly
Take 1 capsule 3 times daily. Swallow the whole capsule with water.
Not for use in children and adolescents under 18 years (see section 4.4 Special warning and precautions for use).
Duration of use
If symptoms worsen or persist after 2 weeks of using the medicinal product, a doctor or a qualified healthcare practitioner should be consulted.
4.3 Contraindications
Hypersensitivity to Horsetail or any of the ingredients
Conditions where a reduced fluid intake is recommended (e.g. severe cardiac
or renal diseases)
4.4 Special warnings and precautions for use
Do not exceed the stated dose
The use in children and adolescents under 18 years of age is not recommended due to lack of adequate data.
If the symptoms worsen during the use of the medicinal product a doctor or a qualified healthcare practitioner should be consulted.
If complaints of symptoms such as fever, dysuria, spasms or blood in the urine occur during the use of the medicinal product, a doctor or a qualified healthcare practitioner should be consulted.
Interaction with other medicinal products and other forms of interaction
4.5
None reported
4.6 Fertility, pregnancy and lactation
Safety during pregnancy and lactation has not been established. Due to the lack of data, use during pregnancy and lactation is not recommended.
Tests on the effects on fertility have not been performed
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
Mild gastrointestinal disturbances such as nausea and diarrhoea Allergic reactions (e.g. rash). The frequency is not known.
If other adverse reactions not mentioned above occur, a doctor or qualified healthcare practitioner should be consulted.
4.9 Overdose
No cases 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 reproductive toxicity, genotoxicity and carcinogenicity have not been performed
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Microcrystalline cellulose Magnesium stearate
Excipients in the extract:
Maltodextrin
Capsule Shell:
Hypromellose
6.2 Incompatibilities
Not applicable.
6.3 Shelf life
2 years
6.4 Special precautions for storage
Do not store above 25°C.
Keep in the original container. Keep the bottle tightly closed.
6.5 Nature and contents of container
Container:
Green Polyethylene terephthalate (PET) bottles with a chiffon green hinge cap (Polypropylene), with an inner seal liner designed to lift ‘n’ peel. The inner seal acts as a tamper evident seal under the cap. The inner seal liner is made up of polyester film, polymer adhesive layer, polyester tab, polyolefin foam, aluminium foil and sealable polyester film.
Pack size: 30 capsules
6.6 Special precautions for disposal
No special requirements.
7 MARKETING AUTHORISATION HOLDER
NBTY Europe Limited Samuel Ryder House Barling Way Nuneaton Warwickshire CV10 7RH United Kingdom
MARKETING AUTHORISATION NUMBER(S)
8
THR 21710/0015
9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
30/01/2012
10 DATE OF REVISION OF THE TEXT
30/01/2012