Naftifine (HCl)

Naftifine (HCl) is antifunfal agent. Naftifine (HCl) is allylamine used topically.


Adult Dose
Dose: 1%
Single Dose: 1 (1)
Frequency: 24 hourly
Route: Topical
Instructions: -
Neonatal
Paedriatic
Dose: 1%
Single Dose: 1 (1)
Frequency: 24 hourly
Route: Topical
Instructions: -
Characteristics
. It is of Synthetic origin and belongs to Allylamine. It belongs to Dermatological Products and Antifungal Agent, Topical pharmacological group.The Molecular Weight of Naftifine (HCl) is 323.90.
Contraindications
Naftifine (HCl) is contraindicated in conditions like Hypersensitivity to any component of product.
Effects
The symptomatic adverse reactions produced by Naftifine (HCl) are more or less tolerable and if they become severe, they can be treated symptomatically, these include Erythema, Redness, Itching, Burning, Dry skin, Local irritation, Stinging.
Indications
Naftifine (HCl) is primarily indicated in conditions like Dermatophyte infections of the nails, Inflammation, Mycoses, Pityriasis versicolor, Skin infections.
Interactions
No data regarding the interactions of Naftifine (HCl) was found.
Interfrence
Risks
Drug should not be given to Paediatrics, and Pregnant Mothers.If prescribing authority justifies the benefits of the drug against the possible damages he/she should reevaluate them and consult the reference material and previous studies.
Storage
Cream, Gel Store Below 40°C. Protect from Sunlight and Heat.
Warnings
Naftifine should be used cautiously during pregnancy only if clearly needed. Avoid the use of occlusive dressings or wrappings unless otherwise directed by the physician. It is for topical use only and not for ophthalmic use.
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