Saturday, 21 November 2009

Heparin-Rotexmedica




Heparin-Rotexmedica may be available in the countries listed below.


Ingredient matches for Heparin-Rotexmedica



Heparin

Heparin sodium salt (a derivative of Heparin) is reported as an ingredient of Heparin-Rotexmedica in the following countries:


  • Germany

International Drug Name Search

Wednesday, 18 November 2009

Durasal



salicylic acid

Dosage Form: topical solution

Package Insert Durasal



Rx only


FOR TOPICAL USE ONLY.


NOT FOR OPHTHALMIC, ORAL OR INTRAVAGINAL USE.



DESCRIPTION


Durasal™ is a topical preparation for treatment of common and plantar warts containing 26% salicylic acid in a film-forming vehicle composed of isopropyl alcohol, butyl acetate, polyvinyl butyral, trimethyl pentanyl diisobutyrate and acrylates copolymer. The pharmacologic activity of Durasal is generally attributed to the keratolytic activity of salicylic acid which is incorporated into a film-forming vehicle designed to cover the wart without the need for a bandage. The structural formula of salicylic acid is:




CLINICAL PHARMACOLOGY


Although the exact mode of action of salicylic acid in the treatment of warts is not known, its activity appears to be associated with its keratolytic action which results in mechanical removal of epidermal cells infected with wart viruses.



INDICATIONS AND USAGE


Durasal is indicated for the topical treatment and removal of common warts and plantar warts.



CONTRAINDICATIONS


Durasal should not be used by diabetics or patients with impaired blood circulation. Durasal should not be used on moles, birthmarks, unusual warts with hair growing from them or warts on the face.



PRECAUTIONS


Durasal is for external use only. Do not permit Durasal to contact eyes or mucous membranes. If contact with eyes or mucous membranes occurs, immediately flush with water for 15 minutes. Durasal should not be allowed to contact normal skin surrounding wart. Treatment should be discontinued if excessive irritation occurs. Durasal is flammable and should be kept away from fire or flame. Keep bottle tightly capped when not in use.



ADVERSE REACTIONS


A localized irritant reaction may occur if Durasal is applied to the normal skin surrounding the wart. Any irritation may normally be controlled by temporarily discontinuing use and by applying the medication only to the wart site when treatment is resumed.



DOSAGE AND ADMINISTRATION


Prior to application of Durasal, soak wart in warm water for five minutes. Remove any loosened tissue by gently rubbing with a brush, wash cloth or emery board. Dry thoroughly. Using the brush applicator supplied, apply twice to entire wart surface, allowing the first application to dry before applying the second. Treatment should be once or twice a day and should continue as directed by physician. Be careful not to apply to surrounding skin. Clinically visible improvement will normally occur during the first or second week of therapy. Maximum resolution may be expected after four to six weeks of drug use.



HOW SUPPLIED


Durasal is supplied in 10ml amber bottles with a brush applicator (NDC 42783-301-10).


Store at controlled room temperature, 15° to 30°C (59° to 86°F).


Manufactured for:

Elorac, Inc.

Vernon Hills, IL 60061


U.S. Patent Pending


6/2009



Durasal (Salicylic Acid, 26%) Wart Remover 10 mL Container Label Principal Display Panel Text:


NDC 42783-301-10


Durasal

solution, 26%

10 mL


FOR TOPICAL USE ONLY

NOT FOR USE IN THE EYES


Rx only




Durasal (Salicylic Acid, 26%) Wart Remover 10 mL Carton Label Principal Display Panel Text:


NDC 42783-301-10


Durasal

solution, 26%

10 mL


FOR TOPICAL USE ONLY

NOT FOR USE IN THE EYES


Rx only










Durasal 
salicylic acid  solution










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)42783-301
Route of AdministrationTOPICALDEA Schedule    








Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
salicylic acid (salicylic acid)salicylic acid260 mg  in 1 mL





Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found


















Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains      














Packaging
#NDCPackage DescriptionMultilevel Packaging
142783-301-101 BOTTLE In 1 CARTONcontains a BOTTLE, WITH APPLICATOR
110 mL In 1 BOTTLE, WITH APPLICATORThis package is contained within the CARTON (42783-301-10)










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other08/03/2009


Labeler - Elorac, Inc. (832590009)

Registrant - Elorac, Inc. (832590009)









Establishment
NameAddressID/FEIOperations
Harmony Labs105803274manufacture
Revised: 02/2010Elorac, Inc.




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Compare Durasal with other medications


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Monday, 16 November 2009

Amlodipine Alter




Amlodipine Alter may be available in the countries listed below.


Ingredient matches for Amlodipine Alter



Amlodipine

Amlodipine besilate (a derivative of Amlodipine) is reported as an ingredient of Amlodipine Alter in the following countries:


  • France

International Drug Name Search

Saturday, 7 November 2009

Marvil




Marvil may be available in the countries listed below.


Ingredient matches for Marvil



Alendronic Acid

Alendronic Acid is reported as an ingredient of Marvil in the following countries:


  • Argentina

  • Peru

International Drug Name Search

Tussamed




Tussamed may be available in the countries listed below.


Ingredient matches for Tussamed



Clobutinol

Clobutinol hydrochloride (a derivative of Clobutinol) is reported as an ingredient of Tussamed in the following countries:


  • Romania

International Drug Name Search

Wednesday, 4 November 2009

Pan




Pan may be available in the countries listed below.


Ingredient matches for Pan



Pantoprazole

Pantoprazole is reported as an ingredient of Pan in the following countries:


  • India

International Drug Name Search