GlaxoSmithKline Voltaren AC Gel 50g

GlaxoSmithKline Voltaren AC Gel 50g

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● Voltaren AC Gel is an analgesic and anti-inflammatory gel containing diclofenac sodium and has excellent transdermal absorbability. ● It is a type that does not contain menthol and does not bother the odor. ● A gel that is not sticky and dries quickly. ● It stretches well and can be easily used on frequently moving parts such as elbows, knees, and wrists. ● There is no need to rub in repeatedly. (If you rub it many times, it may come off.) Check the drug description document with PDF. Additives: diisopropyl adipate, lactic acid, isopropanol, sodium metabisulfite, hydroxyethyl cellulose, hydroxypropyl cellulose
Dosage and administration. Apply an appropriate amount to the affected area 3 to 4 times a day. please. However, do not cover the rubbed area with plastic wrap or other material with poor ventilation. In addition, please do not use other external preparations containing this ingredient together.
Precautions regarding usage and dosage. (1) Please strictly observe the prescribed usage and dosage. (2) This drug does not treat the diseases that cause pain and swelling, but only treats symptoms such as pain and swelling, so use it only if you have symptoms. .. (3) Use this drug only for external use and do not take it internally. (4) Do not use more than 50g per week. (5) Be careful not to get this in your eyes. Should it get in your eyes, immediately wash with water or lukewarm water. If you have severe symptoms, please consult an ophthalmologist. (6) Do not use other external preparations together with the site of use. (7) Do not cover the area to be used with something with poor ventilation (wrap film, straightening belt, etc.) and do not seal it. (8) Wash your hands after use. Formulation / Shape Gel (Gel)

Efficacy Indications Low back pain, shoulder pain associated with stiff shoulders, arthralgia, muscle pain, tendonitis (hand / wrist pain), elbow pain (tennis elbow, etc.), bruise, sprain

Precautions for use Precautions for use 1. Do not use the following people: (1) People who have had allergic symptoms due to this drug or the ingredients of this drug (2) People who have had asthma (3) Pregnant women or people who are thought to be pregnant (4) Under 15 years old Children 2. Do not use on the following parts. (1) Around the eyes, mucous membranes, etc. (2) Weak skin areas (face, head, armpits, etc.) (3) Eczema, rashes, wounds (4) Athlete's foot, rash, etc. or purulent affected area 3. Do not use other topical analgesics and anti-inflammatory agents while using this drug. 4. Please do not use it continuously for a long time. Consultation points for use 1. The following people, please consult your doctor, pharmacist or registered distributor before use. (1) People who are being treated by a doctor (2) People who have had allergic symptoms due to drugs, etc. (3) People who are receiving the following drugs New quinolone antibacterial agents 2. If you experience any of the following symptoms during or after use, you may have side effects. Stop using the product immediately and consult your doctor, pharmacist or registered distributor with this explanation document. Related parts: Symptoms Skin: Rash / redness, itch, rash, swelling, pain, irritation, heat, rough skin, desquamation (dandruff, peeling of skin like red), blisters, pigmentation Serious symptoms may occur. In that case, please see a doctor immediately. Name of symptom… Symptom shock (anaphylaxis)… Immediately after use, itching of the skin, hives, faint voice, swelling, itching of the throat, suffocation, palpitation, cloudiness of consciousness, etc. appear. Contact skin inflammation, photosensitivity ... Rash / redness with strong itching, swelling, irritation, blisters / sores and other severe skin inflammation, pigmentation, and vitiligo appear, including rash / redness and itching. Symptoms such as may spread throughout the body. In addition, symptoms may appear or worsen in areas exposed to sunlight. If symptoms do not improve after using for 3.5 to 6 days, discontinue use and consult a doctor, pharmacist or registered distributor with this explanatory document.

JAN: 4987443330382


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