■Product OverviewManufacturer: Hisamitsu PharmaceuticalProduct Name: Feitas Zα JX 7 PatchesPharmaceutical Classification: Category 2 Specified Controlled SubstancesCategory: OTC DrugPediatric Classification: For Adults (Dosage and administration only for adults aged 15 and over)Drug Form: Patch/PlasterContents: 7 PatchesProduct Description: A transdermal anti-inflammatory analgesic patch containing 2.0% diclofenac sodium as the active ingredient.[Expiration Date]More than 1 year remaining from the date of shipment.JAN Code: 4987188123805Product Code: 011407891
■Date of Initial Package Insert Creation and Revision, Package Insert Version NumberInitial Creation: -Revision: -
■Features- A transdermal anti-inflammatory analgesic patch containing 2.0% diclofenac sodium as the active ingredient.- Contains 3.5% l-menthol for enhanced efficacy.- Provides excellent relief for severe pain in shoulders, neck, lower back, joints, and muscles.- Lightly scented, so it is not noticeable during sleep or in public.- Stretches in all directions for a perfect fit on the skin.
■Prohibitions(Failure to follow these instructions may worsen current symptoms or increase the risk of side effects.)1. Do not use on the following individuals.(1) Individuals who have experienced allergic reactions to this product or its ingredients.(2) Individuals who have experienced asthma.(3) Pregnant women or women who may be pregnant.(4) Children under 15 years of age.2. Do not use on the following areas.(1) Around the eyes, mucous membranes, etc.(2) Eczema, rashes, wounds.(3) Areas with athlete's foot, ringworm, or infected wounds.3. Do not use other topical analgesics or anti-inflammatory drugs concurrently while using this product.4. Do not use continuously for more than 2 weeks.
■Consultation1. The following individuals should consult a doctor, pharmacist, or registered seller before use.(1) Individuals receiving medical treatment.(2) Individuals using other medications.(3) Individuals who have experienced allergic reactions to drugs, etc.(4) Individuals who have experienced rashes or other reactions to patch formulations.(5) Individuals diagnosed with the following conditions: peptic ulcer, blood disorders, liver disease, kidney disease, hypertension, heart disease, influenza.(6) Individuals receiving the following medications: quinolone antibiotics, triamterene, lithium, methotrexate, non-steroidal anti-inflammatory drugs, corticosteroids, diuretics, cyclosporine, selective serotonin reuptake inhibitors.(7) Elderly individuals.2. If any of the following symptoms appear after use, discontinue use immediately and consult a doctor, pharmacist, or registered seller with this package.Affected Area | SymptomsSkin | Rash/redness, itching, rash, swelling, rough skin, irritation, pigmentation, blisters, scaling (fine shedding of skin flakes)
In rare cases, the following severe symptoms may occur. In such cases, seek immediate medical attention.Name of Symptom | SymptomsShock (anaphylaxis) | Immediately after use, symptoms such as itchy skin, hives, hoarseness, sneezing, itchy throat, difficulty breathing, palpitations, and clouded consciousness may occur.Contact dermatitis, photosensitivity | Severe skin inflammation symptoms such as severe itching, rash/redness, swelling, irritation, blisters/sores at the application site, pigmentation, and white spots may appear. In some cases, symptoms such as rash/redness and itching may spread throughout the body. Symptoms may also appear or worsen in areas exposed to sunlight.
3. If symptoms do not improve after 5-6 days of use, discontinue use and consult a doctor, pharmacist, or registered seller with this package.
■Efficacy and EffectsLower back pain, muscle pain, shoulder pain associated with stiff shoulders, joint pain, tenosynovitis (pain in hands/wrists), elbow pain (e.g., tennis elbow), bruises, sprains.
■Dosage and AdministrationRemove the plastic film and apply 1 to 2 patches to the affected area once a day. However, do not use more than 2 patches at a time. Do not use other external medications containing the same active ingredient concurrently.
| Product # | TH011407891 |
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