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Voltaren Emulgel 1% 50g gel




The instruction for medical use


the Trade name

Emulgel Mezhdunarodnoye Voltarenum the unlicensed

name Diclofenac Dosage Form Gel for external use of 1%


of 100 g of drug contain

active agent: diclofenac diethyl amine of 1.16 g 1.00 g of diclofenac of sodium

excipients are equivalent: carbomers (karbopol 974 P), a macrogoal cetostearyl ether (tsetomakrogol 1000), kokoit kaprilokaprat (tsetiol HP), diethyl amine, isopropyl alcohol, liquid paraffin, mineral oil (heavy liquid paraffin), cream aromatic 45, propylene glycol (1.2 propylene glycol distilled), the water purified.

The description

Soft, uniform creamy gel from white till yellowish color.

Pharmacotherapeutic group

Non-steroidal anti-inflammatory drugs for topical administration. Diclofenac.

The ATX M02AA15 code

the Pharmacological

Pharmacokinetics At properties the recommended way of drawing Emulgelya Voltarenum is absorbed no more than 6% of diclofenac. At local putting drug of 99.7% of diclofenac contacts proteins of serum and generally (99.4%) albumine. Diclofenac collects in the skin operating as a source of the slowed-down release of substance in the subject fabrics. From there diclofenac is distributed and remains mainly in the deep inflamed fabrics where reaches concentration by 20 times exceeding concentration in plasma. Biotransformation of diclofenac is carried out partially by a glyukoronidation of an invariable molecule, however, the most part of the arrived substance is exposed to single or multiple hydroxylation with formation of phenolic metabolites which turn into glucuronic conjugates. The general system clearance of diclofenac in blood plasma averages 263&plusmn, 56 ml/min., and final elimination half-life of diclofenac make 1-2 hours, are removed mainly with urine.

A pharmacodynamics

Active component diclofenac the non-steroidal anti-inflammatory drug having analgeziruyushchy and anti-inflammatory properties. The main mechanism of effect of diclofenac consists in suppression of biosynthesis of prostaglandins namely, not selectively oppressing type cyclooxygenase 1 and 2, breaks metabolism of arachidonic acid.

Emulgel Voltarenum is used for elimination of a pain syndrome and reduction of puffiness connected with inflammatory process.

At the expense of an emulsion form Emulgel Voltarenum easily gets through skin, quickly reaching effective concentration, and cooling a gel component and calming, promotes long influence of active agent.


– traumatic injuries of sinews, ligaments, muscles and joints without disturbance of integrity of integuments (bruises, stretchings, dislocations, hematomas), a back pain

– an osteoarthritis

– the bursitis, tendonit, a periarthritis

– infectious, traumatic arthritis

– a pseudorheumatism as a part of complex therapy

– neuralgia, myalgias and others a disease basic dvigatelnogo the device, followed by inflammation and a pain syndrome

A route of administration and doses


To adults and children 12 years 3-4 times a day are more senior, slightly rubbing in skin on sore parts of the body. After putting drug it is recommended to wash up hands.

A single dose – 2-4 g. Duration of treatment depends on indications and efficiency of therapy. It is not necessary to use drug more than 14 days in a row at defeat of soft tissues or a rheumatic disease of soft tissues more than 21 day in case of the pain caused by arthritis (if the doctor did not appoint other scheme of treatment).

In case of use of drug without appointment, it is necessary to see a doctor if within 7 days use, the condition of the patient did not change.

Side effects

Often (& ge, 1/100, but & lt, 1/10)

– contact dermatitis (rash, an erythema, eczema of naggers)

it is rare (& ge, 1/10000, но&lt, 1/1000)

– bullous dermatitis

Very seldom (& lt, 1/10000)

– pustulous rashes

– reactions of hypersensitivity (urticaria, a Quincke’s edema)

– bronkhospastichesky reactions, asthma – reactions of a photosensitization of the Contraindication – hypersensitivity to diclofenac or other components of drug – tendency to emergence of attacks of bronchial asthma, urticaria or acute rhinitises at use of acetylsalicylic acid or other non-steroidal anti-inflammatory drugs (aspirinovy asthma) – disturbance of integrity of integuments – pregnancy and the period of a lactation – children’s age up to 12 years

Medicinal interactions

As system absorption of a diklovenak at topical administration of drug very low, emergence of interaction is improbable.

The special

instructions Voltarenum Emulgel should be applied only to the uninjured healthy skin, avoiding hit on the inflamed sites and open wounds.

It is not necessary to allow hits of drug in eyes and on mucous membranes.

It is not necessary to apply inside. It is not necessary to apply under an occlusive occlusive bandage.

Emulgel Voltarenum contains benzyl benzoate as a part of cream aromatic 45 and also propylene glycol which can cause weak local irritation of skin in some patients.

Influence on ability to run the vehicle or other potentially dangerous mechanisms

does not influence ability to run the vehicle or other potentially dangerous mechanisms.


Symptoms: the overdose at topical administration of drug is improbable. At accidental intake such complications as hypotonia, a renal failure, spasms, irritation of digestive tract and respiratory depression can be observed. Treatment: gastric lavage, intake of activated carbon, symptomatic therapy.

A form of release and packing

On 50 g of drug in aluminum tubas with a protective aluminum membrane, with the screw-on plastic cover having a ledge for perforation of a membrane from outer side or in the laminated tubas (polyethylene of low density, aluminum, polyethylene of high density) with a shoulder and a tselnolity figured protective membrane from polyethylene of high density and the polypropylene screw-on cover. The cover from outer side is supplied with a key (deepening with ledges) for opening of a protective membrane of a tuba.

On 1 tuba together with the instruction for medical use in the state and Russian languages place in a pack from cardboard.

To Store storage conditions at a temperature not over 30 With

to Store out of children’s reach!

The period of storage

Drug should not be used 3 years after the expiry date specified on packing.

Prescription status

Without prescription

of Proizvoditel Novartis Pharm Produktsions GmbH, Germany

the Name and the country of the owner of the registration certificate

of Novartis Konsyyumer Hels SA, Switzerland

the Address of the organization accepting in the territory of the Republic of Kazakhstan claims from the consumer on quality of a product
Almaty, Luganskogo St., 96
ph. 8-800-080-0650 (free from all stationary phones across the Republic of Kazakhstan)
fax: (727) 244-26-51

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