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BETNOLAND OINTMENT

Home Medicines
Topical Corticosteroid

BETNOLAND OINTMENT

REGULATORY INFORMATION

MAH & BR: Prolifepharma BV, The Netherlands, EU GMP Certified
Manufacturing site Italy
Language EN
Reference Medicinal Product Diprolene (Schering-Plough, USA)
PRODUCT INFORMATION
Active Substance Betamethasone Dipropionate
Strength | Dosage Form 0.1% Ointment
Indications
  • Betnoland 0.1% Ointment is used on the surface of the skin to reduce the redness and itchiness caused by certain skin problems.
  • In adults and children, Betnoland 0.1% Ointment is used to treat skin problems, including:
  • eczema, and all types of dermatitis and psoriasis of the scalp, hands and feet.
Posology
  • Usually for adults and children, a thin layer of Betnoland 0.1% Ointment should be rubbed into the affected area of skin twice a day.
  • You should always follow these instructions when using Betnoland 0.1% Ointment:
  • Do not use the cream on your face for more than 5 days.
  • Do not use a large amount of Ointment on large areas of the body, open wounds or areas of the body where joints bend for a long time (for example every day for many weeks or months).
  • Do not use Betnoland 0.1% Ointment on any part of your child’s body for more than 5 days.
  • Refer to your doctor or healthcare practitioner before using this medication
Route of Administration Percutaneous
Presentations 1 tube of 30 gm Ointment
Shelf-life 5 years
Storage conditions Do not store above 30°C.
ATC Code D07CC01 Betamethasone Dipropionate
Pharmacotherapeutic Group Topical Corticosteroid

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