BP CLEANSER  - benzoyl peroxide emulsion 
River’s Edge Pharmaceuticals, LLC

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BP 4.25% Cleanser(benzoyl peroxide 4.25%)

Active Ingredients

Benzoyl peroxide 4.25%

Purpose

Acne treatment

Uses

For the treatment of acne.

Warnings

For External Use Only.
When using this product

Do not use if you

When using this product

Stop and ask a doctor if

KEEP THIS AND ALL DRUGS OUT OF THE REACH OF CHILDREN.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions


Sensitivity test for a new user

Other Information

Store at 25°C (77°F); excursions permitted to 15°-30°C (59°-86°F).

Inactive Ingredients

allantoin, aloe barbadensis leaf extract, benzyl alcohol, camellia oleifera leaf (green tea) extract, carbomer, cetyl alcohol, disodium laureth sulfosuccinate, glycerin, glyceryl stearate, magnesium aluminum silicate, octoxynol-13, panthenol, PEG-100 stearate, PPG-14 palmeth-60 hexyl dicarbamate, propylene glycol, purified water, sodium citrate, sodium hyaluronate, triethanolamine, and xanthan gum.

Questions? Comments?

Call 1-866-934-6025

label

BP CLEANSER 
benzoyl peroxide   emulsion
Product Information
Product TypeHUMAN OTC DRUGNDC Product Code (Source)68032-602
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (BENZOYL PEROXIDE) BENZOYL PEROXIDE42.5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALLANTOIN 
ALOE VERA LEAF 
BENZYL ALCOHOL 
GREEN TEA LEAF 
CARBOMER 1342 
CETYL ALCOHOL 
DISODIUM LAURETH SULFOSUCCINATE 
GLYCERIN 
GLYCERYL MONOSTEARATE 
MAGNESIUM ALUMINUM SILICATE 
OCTOXYNOL 9 
PANTHENOL 
POLYOXYL 100 STEARATE 
PROPYLENE GLYCOL 
WATER 
SODIUM CITRATE 
HYALURONATE SODIUM 
TROLAMINE 
XANTHAN GUM 
Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#NDCPackage DescriptionMultilevel Packaging
168032-602-16473 mL In 1 BOTTLENone

Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333D03/23/2011

Labeler - River’s Edge Pharmaceuticals, LLC (133879135)
Revised: 03/2011River’s Edge Pharmaceuticals, LLC