NADIBACT PLUS CREAM 7.5GM

Manufacturer : CIP-CIPLA LTD
Composition : MICONAZOLE-2% W/W+MOMETASONE-0.1% W/W+NADIFLOXACIN-1% W/W
Dose Form : CREAM
Description : NADIBACT PLUS CREAM 7.5GM
Route Of Administration : TOPICAL
Pack : 1
In stock
SKU
NAD0030
₹77.55
Manufacturer : CIP-CIPLA LTD
Composition : MICONAZOLE-2% W/W+MOMETASONE-0.1% W/W+NADIFLOXACIN-1% W/W
Dose Form : CREAM
Description : NADIBACT PLUS CREAM 7.5GM
Route Of Administration : TOPICAL
Pack : 1

Drug Ingredient Information

MICONAZOLE-2% W/W+MOMETASONE-0.1% W/W+NADIFLOXACIN-1% W/W

MICONAZOLE

Information for patients
Drug Information MICONAZOLE NITRATECream is a medicine which is used to effectively treat and relieve Athlete’s Foot. The cream contains miconazole nitrate which works by destroying both the fungus that causes the infection and some of the associated bacteria which may also be present. It also has moisturising properties to help soothe cracked, red skin caused by Athlete’s Foot.This medicine is for use in adults and children of all ages.
Drug Alert
Alert ¦ If you have ever had a bad reaction to any of the ingredients. If this applies to you, get advice from a doctor or pharmacist without using MICONAZOLE NITRATECream
Before Consuming the Medicine
Avoid Drug ¦ If you have ever had a bad reaction to any of the ingredients. If this applies to you, get advice from a doctor or pharmacist without using MICONAZOLE NITRATECream
Drug Special Care ¦ Do not let the cream get into your eyes. ¦ If you experience any irritation or sensitivity to the cream, stop using this medicine.
Drug Drug Interactions ¦ Oral anticoagulants (drugs used to thin the blood, such as warfarin).
Drug Pregnancy Interaction ¦ Ask your doctor or pharmacist for advice before using this medicine if you are pregnant or breast-feeding.
Drug Breast feeding Interaction ¦ Ask your doctor or pharmacist for advice before using this medicine if you are pregnant or breast-feeding.
Drug Machinery Interaction
Drug More Information ¦ Benzoic acid (E210) can mildly irritate the skin, eyes and mucosal membranes. ¦ Butylated hydroxyanisole (E320) may cause local skin reactions (e.g. contact dermatitis), or irritation to the eyes and mucous membranes.
How to take the Medicine
Consumption Info ¦ Each tube of cream is sealed – use the cap to pierce the seal ¦ For cutaneous use only, which means it is applied directly to the affected area of skin. ¦ Do not use more often than the stated.
Drug quanitty Adults and children of all ages:Apply the cream to the infected skin twice a day (e.g. at night and in the morning). ¦ Continue treatment for 10 days after all the symptoms have cleared to prevent them from coming back. ¦ If symptoms persist talk to your doctor.
Drug Dose ¦ Wash the infected area and dry it well. As many skin conditions are contagious, you should keep a towel and flannel for your own use and not share it so that you do not infect anyone else. ¦ Apply the cream onto the infected area and surrounding skin. ¦ Wash your hands carefully after applying the cream to avoid spreading the infection to other parts of the body or to other people. Similarly, clothing which comes into contact with the infected areas, such as socks, should be washed and changed frequently.
Excess Drug Consumption If anyone accidentally swallows MICONAZOLE NITRATECream, contact a doctor or your nearest Accident and Emergency department (Casualty), taking this leaflet and pack with you
Forgot Drug Consumption If you forget to use a dose, use the next dose when needed. Do not use a double dose.
Stop Drug Consumption
Possible Side Effects
General Information
Common Drug Side Effects
Rare Drug Side Effects ¦ Sensitivity reactions (such as rash) at the application site. If this occurs stop using the medicine
Very Rare Drug Side Effects ¦ Severe allergic reactions including swelling of the face, lips, tongue or throat. ¦ Light headedness, generalised itch, wheezing or difficulty in breathing ¦ Allergic reactions such as a skin rash, itchiness, hives, swelling, redness or a burning feeling
Drug Side Effects Symptoms
How to Store the Medicine
How to Store the Medicine Do not store above 25ºC.Keep the product out of the reach and sight of children. Do not use your medicine after the date shown as the expiry date on the packaging. Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment

MOMETASONE

Information for patients
Drug Information MOMETASONE is one of a group of medicines called topical corticosteroids. It is classified as a “potent corticosteroid”. These medicines are put on the surface of the skin to reduce the redness and itchiness caused by certain skin problems.In adults and children, MOMETASONE is used to reduce redness and itchiness caused by certain skin problems called psoriasis or dermatitis.Psoriasis is a skin disease in which itchy, scaly, pink patches develop on the elbows, knees, scalp and other parts of the body. Dermatitis is a condition brought on by the skin reacting to outside agents e.g. detergents, causing the skin to become red and itchy.
Drug Alert
Alert no data available
Before Consuming the Medicine
Avoid Drug – if you are allergic (hypersensitive) to mometasone furoate, any of the other ingredients of MOMETASONE or to similar medicines. – on any other skin problems as it could make them worse especially rosacea (a skin condition affecting the face) acne skin atrophy (thinning of the skin) dermatitis around the mouth genital itching nappy rash cold sores chickenpox shingles warts ulcerated skin wounds other skin infections. Ask your doctor or pharmacist if you are not sure.
Drug Special Care if your skin becomes irritated or sensitive after using MOMETASONE, you should stop using it and tell your doctor
Drug Drug Interactions no data available
Drug Pregnancy Interaction You should tell your doctor if you are pregnant or breast-feeding, before you start using MOMETASONE
Drug Breast feeding Interaction You should tell your doctor if you are pregnant or breast-feeding, before you start using MOMETASONE
Drug Machinery Interaction no data available
Drug More Information no data available
How to take the Medicine
Consumption Info no data available
Drug quanitty no data available
Drug Dose Always use MOMETASONE exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure. MOMETASONE is not recommended for children under the age of 2. Usually for adults and children, a thin layer of MOMETASONE should be gently rubbed into the affected area of skin once a day. You should always follow these instructions when using MOMETASONE: –Do not use the on your face for more than 5 days –Do not apply the to children, on any part of their body, for more than 5 days. –Do not put the under your child’s nappy, as this makes it easier for the active drug to pass through the skin and possibly cause some unwanted effects. –You should check with your doctor before covering the treated areas with a bandage or plaster. Treated areas on the face or in children should not be covered with a bandage or plaster. –You should not use a large amount of on large areas of the body for a long time (for example every day for many weeks or months). –Do not use in or around your eyes, including eye-lids
Excess Drug Consumption If you (or somebody else) accidentally swallows the , it should not produce any problems. However, if you are worried, you should see your doctor. If you use the more often than you should, or on large areas of the body, it can affect some of your hormones. In children, this may affect their growth and development. If you have not used the cream as you were told to do and have used it too often and/or for a long time, you should tell your doctor.
Forgot Drug Consumption If you forget to use your at the right time, use it as soon as you remember, then carry on as before.
Stop Drug Consumption If you have been using MOMETASONE for a long time and your skin problem seems to have got better, you should not suddenly stop using the . If you do, you may find that your skin becomes red and you may notice stinging or burning. To avoid this, you should speak to your doctor as he will gradually reduce how often you need to use the until you stop treatment altogether.
Possible Side Effects
General Information no data available
Common Drug Side Effects –allergic skin reactions –bacterial and secondary skin infections –acne –inflammation and/ or infection of the hair follicles –thinning of the skin –red marks with associated prickly heat –loss of skin colour –burning –stinging –itching –tingling –excessive hair growth –softening of the skin and stretch marks
Rare Drug Side Effects no data available
Very Rare Drug Side Effects no data available
Drug Side Effects Symptoms no data available
How to Store the Medicine
How to Store the Medicine The should be stored between 2 and 30°C. Keep out of the reach of children. Do not use MOMETASONE after the expiry date which is stamped on the pack.

NADIFLOXACIN

Information for patients
Drug Information For topical treatment of mild to moderate inflammatory forms of acne vulgaris
Drug Alert
Alert The product should not be applied to broken skin (cuts and abrasions). There is no data covering the safety of concomitant treatment with other acne medications (e.g. benzoyl peroxide), and nadifloxacin should therefore be used as a monotherapeutic only. nadifloxacin Cream contains: stearyl alcohol and cetyl alcohol, which may cause local skin reactions (e.g. contact dermatitis) and benzalkonium chloride, which may be irritant and may cause skin reactions.
Before Consuming the Medicine
Avoid Drug nadifloxacin is contraindicated in known hypersensitivity to nadifloxacin or any excipient of the product.
Drug Special Care The safety and effectiveness of nadifloxacin cream have not been studied sufficiently in children below the age of 14 years. Therefore nadifloxacin should not be used in patients of this age group. Contact with the eyes or other mucous membranes should be avoided. Contact with nadifloxacin requires immediate flushing of eyes or mucous membranes with warm water. Hands should be washed after applying the cream in order to avoid unintentional application to other areas. Photosensitivity reactions have been known to develop under therapy with other quinolones administered systemically. While several studies in animals and man have shown neither phototoxic nor photoallergic potentials for the active ingredient nadifloxacin, the cream base may have an enhancing effect on photosensitivity. Moreover no experience is available on prolonged exposure to sunlight or artificial UV light under nadifloxacin. Patients using nadifloxacin cream should therefore avoid exposure to artificial UV irradiation (UV lamps, sun bed, solarium) as a matter of principle and exposure to sunlight whenever possible. If hypersensitivity reactions (manifesting as itching, erythema, papules, vesicles) or severe irritation occurs, use of medication should be discontinued.
Drug Drug Interactions Absorption of nadifloxacin after application of nadifloxacin to the human skin is very low (see 5.2 Pharmacokinetic properties) and therefore interaction with systemic medication given concurrently is unlikely. There is no evidence to indicate that the efficacy of systemically administered drugs is influenced by the topical use of nadifloxacin Cream. nadifloxacin may cause skin irritation and therefore it is possible that the concomitant use of peeling agents, astringents or products containing irritating substances such as aromatic and alcoholic agents may result in increased skin irritation.
Drug Pregnancy Interaction For nadifloxacin cream, no clinical data on exposed pregnancies are available. Animal studies do not indicate direct or indirect harmful effects with respect to pregnancy, embryonal, foetal development, parturition or postnatal development Caution should be exercised when prescribing to pregnant women.
Drug Breast feeding Interaction Nadifloxacin is known to be excreted in milk and therefore nadifloxacin Cream should not be used during lactation. Under no circumstances must breast-feeding women apply nadifloxacin on their chest
Drug Machinery Interaction Neither the pharmacodynamic profile nor clinical experience suggest any effect on the ability to drive or use machines.
Drug More Information no data available
How to take the Medicine
Consumption Info no data available
Drug quanitty no data available
Drug Dose nadifloxacin Cream should be applied to the acne lesions twice daily as a thin film, i.e. once in the morning and once in the evening before retiring, after cleaning and carefully drying the affected areas. Care should be taken to avoid the eyes and lips. To avoid infections,nadifloxacin cream should be applied with a cotton bud. nadifloxacin should not be used with occlusive dressing. Treatment with nadifloxacin Cream should be applied for up to 8 (eight) weeks. nadifloxacin should not be used in patients under 14 years of age.
Excess Drug Consumption nadifloxacin Cream is not to be taken orally and is for cutaneous use only. Excessive repetitive applications do not accelerate or improve therapeutic outcome but rather involve the risk of marked redness or discomfort. In rats and mice oral nadifloxacin showed very low acute toxicity with minimum lethal doses exceeding 5000 mg/kg body weight. Nevertheless, an appropriate method of gastric emptying should be considered unless the amount of nadifloxacin accidentally ingested is small.
Forgot Drug Consumption Contact Your doctor
Stop Drug Consumption Do not stop the drug untill your doctor says you to do so.
Possible Side Effects
General Information no data available
Common Drug Side Effects pruritus
Rare Drug Side Effects papules, dry skin, contact dermatitis, skin irritation, skin warm. Vascular disorders
Very Rare Drug Side Effects no data available
Drug Side Effects Symptoms no data available
How to Store the Medicine
How to Store the Medicine No special precautions for storage.

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