BP WASH- benzoyl peroxide emulsion 
A-S Medication Solutions

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BP Wash 2.5% (benzoyl peroxide 2.5%)

Active ingredient​

Benzoyl peroxide 2.5%

Purpose​

Acne treatment

Use​

For the treatment of acne

Warnings

For external use only

Do not use if you


When using this product

Stop use and ask a doctor if irritation becomes severe.

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

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

Directions

Other information​

Store at 15°-30°C (59°-86°F).

Inactive ingredients​

carbomer, cetearyl alcohol, cocamidopropyl betaine, dimethyl isosorbide, hydrogenated castor oil, imidurea, methylparaben, mineral oil, PEG-14M, salicylic acid, sodium cocoyl isethionate, sodium hydroxide, titanium dioxide, water, zea mays (corn) starch

Questions?

1-855-899-4237

HOW SUPPLIED

Product: 50090-6591

NDC: 50090-6591-0 227 g in a BOTTLE

BP WASH- benzoyl peroxide emulsion

Label Image
BP WASH 
benzoyl peroxide emulsion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50090-6591(NDC:24470-911)
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE25 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
CARBOMER HOMOPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: F68VH75CJC)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)  
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
IMIDUREA (UNII: M629807ATL)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
MINERAL OIL (UNII: T5L8T28FGP)  
POLYETHYLENE OXIDE 600000 (UNII: 2126FD486L)  
SALICYLIC ACID (UNII: O414PZ4LPZ)  
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
WATER (UNII: 059QF0KO0R)  
STARCH, CORN (UNII: O8232NY3SJ)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50090-6591-0227 g in 1 BOTTLE; Type 0: Not a Combination Product08/15/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00608/15/2011
Labeler - A-S Medication Solutions (830016429)
Establishment
NameAddressID/FEIBusiness Operations
A-S Medication Solutions830016429RELABEL(50090-6591)

Revised: 11/2023
Document Id: f6e37a9c-c563-4ebc-ae92-52ca1b882422
Set id: 264b209b-4864-47d8-a26c-7bba3c27e9aa
Version: 6
Effective Time: 20231108
 
A-S Medication Solutions