Wednesday, 4 November 2009

Benzoyl Peroxide Cleanser





Dosage Form: solution
Benzoyl Peroxide Cleanser 3%, 6% and 9%

Rx Only



Benzoyl Peroxide Cleanser Description


Benzoyl Peroxide Cleanser 3%, 6%, and 9% are topical, gel-based, benzoyl peroxide containing preparations for use in the treatment of acne vulgaris. Benzoyl peroxide is an oxidizing agent that possesses antibacterial properties and is classified as a keratolytic.


Benzoyl peroxide (C14H10O4) is represented by the following chemical structure:



Benzoyl Peroxide Cleanser 3%, 6% and 9% contain hydrous benzoyl peroxide 3%, 6% and 9% as the active ingredient in a vehicle consisting of: alpha olefin sulfonate, cetostearyl alcohol, glycerin, glyceryl monostearate SE, methylparaben, phosphoric acid, propylene glycol, sodium PCA, white petrolatum and purified water.



Benzoyl Peroxide Cleanser - Clinical Pharmacology


The mechanism of action of benzoyl peroxide is not totally understood but its antibacterial activity against Propionibacterium acnes is thought to be a major mode of action. In addition, patients treated with benzoyl peroxide show a reduction in lipids and free fatty acids, and mild desquamation (drying and peeling activity) with simultaneous reduction in comedones and acne lesions. Little is known about the percutaneous penetration, metabolism, and excretion of benzoyl peroxide, although it has been shown that benzoyl peroxide absorbed by the skin is metabolized to benzoic acid and then excreted as benzoate in the urine. There is no evidence of systemic toxicity caused by benzoyl peroxide in humans.



Indications and Usage for Benzoyl Peroxide Cleanser


Benzoyl Peroxide Cleanser 3%, 6%, and 9% is indicated for the topical treatment of acne vulgaris.



Contraindications


These preparations are contraindicated in patients with a history of hypersensitivity to any of their components.



Warnings


When using this product, avoid unnecessary sun exposure and use a sunscreen.



Precautions



General


For external use only. If severe irritation develops, discontinue use and institute appropriate therapy. After reaction clears, treatment may often be resumed with less frequent application. These preparations should not be used in or near the eyes or on mucous membranes.



Information for patients


Avoid contact with eyes, eyelids, lips and mucous membranes. If accidental contact occurs, rinse with water. Contact with any colored material (including hair and fabric) may result in bleaching or discoloration. If excessive irritation develops, discontinue use and consult your physician.



Carcinogenesis, mutagenesis, impairment of fertility


Data from several studies employing a strain of mice that are highly susceptible to developing cancer suggest that benzoyl peroxide acts as a tumor promoter. The clinical significance of these findings to humans is unknown. Benzoyl peroxide has not been found to be mutagenic (Ames Test) and there are no published data indicating it impairs fertility.



Pregnancy


Teratogenic effects

Pregnancy Category C: Animal reproduction studies have not been conducted with benzoyl peroxide. It is not known whether benzoyl peroxide can cause fetal harm when administered to a pregnant woman or can effect reproduction capacity. Benzoyl peroxide should be used by a pregnant woman only if clearly needed. There are no available data on the effect of benzoyl peroxide on the later growth, development and functional maturation of the unborn child.



Nursing mothers


It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when benzoyl peroxide is administered to a nursing woman.



Pediatric use


Safety and effectiveness in children have not been established.



Adverse Reactions


Allergic contact dermatitis and dryness have been reported with topical benzoyl peroxide therapy.



Overdosage


If excessive scaling, erythema or edema occurs, the use of these preparations should be discontinued. To hasten resolution of the adverse effects, cool compresses may be used. After symptoms and signs subside, a reduced dosage schedule may be cautiously tried if the reaction is judged to be due to excessive use and not allergenicity.



Benzoyl Peroxide Cleanser Dosage and Administration


Benzoyl Peroxide Cleansers: Wash affected areas once or twice daily, or as directed by your dermatologist. Avoid contact with eyes or mucous membranes. Wet skin and liberally apply to areas to be cleansed, massage gently into skin for 10 to 20 seconds working into a full lather, rinse thoroughly and pat dry. If drying occurs, it may be controlled by rinsing cleanser off sooner or using less often.



How is Benzoyl Peroxide Cleanser Supplied


Benzoyl Peroxide Cleanser 3%

6 oz. (170 g) tube - NDC 68462-411-38

12 oz. (340 g) bottle - NDC 68462-411-34


Benzoyl Peroxide Cleanser 6%

6 oz. (170 g) tube - NDC 68462-412-38

12 oz. (340 g) bottle - NDC 68462-412-34


Benzoyl Peroxide Cleanser 9%

6 oz. (170 g) tube - NDC 68462-413-38

12 oz. (340 g) bottle - NDC 68462-413-34



Store at 15° to 25°C (59° to 77°F). [see USP Controlled Room Temperature].



Manufactured by:


Glenmark Generics Ltd.

Colvale-Bardez, Goa 403 513, India


Manufactured for:



Glenmark Generics Inc., USA

Mahwah, NJ 07430


Questions? 1 (888)721-7115

www.glenmarkgenerics.com


February 2009



3% Principal Display Panel




6% Principal Display Panel




9% Principal Display Panel










BENZOYL PEROXIDE 
benzoyl peroxide  solution










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)68462-411
Route of AdministrationTOPICALDEA Schedule    








Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (BENZOYL PEROXIDE)BENZOYL PEROXIDE3 g  in 100 mL






















Inactive Ingredients
Ingredient NameStrength
CETOSTEARYL ALCOHOL 
GLYCERIN 
GLYCERYL MONOSTEARATE 
METHYLPARABEN 
PHOSPHORIC ACID 
PROPYLENE GLYCOL 
SODIUM PYRROLIDONE CARBOXYLATE 
PETROLATUM 
WATER 


















Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains      














Packaging
#NDCPackage DescriptionMultilevel Packaging
168462-411-38177.4 mL In 1 TUBENone
268462-411-34354.9 mL In 1 BOTTLENone










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved drug other03/20/2009







BENZOYL PEROXIDE 
benzoyl peroxide  solution










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)68462-412
Route of AdministrationTOPICALDEA Schedule    








Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (BENZOYL PEROXIDE)BENZOYL PEROXIDE6 g  in 100 mL






















Inactive Ingredients
Ingredient NameStrength
CETOSTEARYL ALCOHOL 
GLYCERIN 
GLYCERYL MONOSTEARATE 
METHYLPARABEN 
PHOSPHORIC ACID 
PROPYLENE GLYCOL 
SODIUM PYRROLIDONE CARBOXYLATE 
PETROLATUM 
WATER 


















Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains      














Packaging
#NDCPackage DescriptionMultilevel Packaging
168462-412-38177.4 mL In 1 TUBENone
268462-412-34354.9 mL In 1 BOTTLENone










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved drug other03/20/2009







BENZOYL PEROXIDE 
benzoyl peroxide  solution










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)68462-413
Route of AdministrationTOPICALDEA Schedule    








Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (BENZOYL PEROXIDE)BENZOYL PEROXIDE9 g  in 100 mL






















Inactive Ingredients
Ingredient NameStrength
CETOSTEARYL ALCOHOL 
GLYCERIN 
GLYCERYL MONOSTEARATE 
METHYLPARABEN 
PHOSPHORIC ACID 
PROPYLENE GLYCOL 
SODIUM PYRROLIDONE CARBOXYLATE 
PETROLATUM 
WATER 


















Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains      














Packaging
#NDCPackage DescriptionMultilevel Packaging
168462-413-38177.4 mL In 1 TUBENone
268462-413-34354.9 mL In 1 BOTTLENone










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved drug other03/20/2009


Labeler - Glenmark Generics Inc., USA (835917282)









Establishment
NameAddressID/FEIOperations
Glenmark Generics Limited677318665ANALYSIS, MANUFACTURE
Revised: 12/2009Glenmark Generics Inc., USA

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