Label: BP WASH- benzoyl peroxide emulsion
- NDC Code(s): 24470-900-04, 24470-900-05, 24470-900-08
- Packager: CINTEX SERVICES, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated December 12, 2022
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- Active ingredient
- Purpose
- Use
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Warnings
For external use only
Do not use if you- have very sensitive skin
- are sensitive to benzoyl peroxide
When using this product- skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.
- avoid unnecessary sun exposure and use a sunscreen
- avoid contact with the eyes, lips, and mouth
- avoid contact with hair and dyed fabrics, which may be bleached by this product
- skin irritation may occur, characterized by redness, burning, itching, peeling, or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration.
Stop use and ask a doctor if irritation becomes severe. - KEEP OUT OF REACH OF CHILDREN
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Directions
- clean the skin thoroughly before applying this product
- cover the entire affected area with a thin layer and rinse thoroughly one to three times daily
- because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
- if bothersome dryness or peeling occurs, reduce application to once a day or every other day.
- if going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor.
- Other information
- Inactive ingredients
- Questions?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BP WASH
benzoyl peroxide emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:24470-900 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE 50 mg in 1 g Inactive Ingredients Ingredient Name Strength DIMETHYL ISOSORBIDE (UNII: SA6A6V432S) SODIUM HYDROXIDE (UNII: 55X04QC32I) METHYLPARABEN (UNII: A2I8C7HI9T) POLYETHYLENE OXIDE 600000 (UNII: 2126FD486L) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) WATER (UNII: 059QF0KO0R) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493) HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY) IMIDUREA (UNII: M629807ATL) MINERAL OIL (UNII: T5L8T28FGP) SALICYLIC ACID (UNII: O414PZ4LPZ) STARCH, CORN (UNII: O8232NY3SJ) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:24470-900-04 113 g in 1 BOTTLE; Type 0: Not a Combination Product 12/15/2011 2 NDC:24470-900-05 142 g in 1 BOTTLE; Type 0: Not a Combination Product 12/15/2011 01/31/2022 3 NDC:24470-900-08 227 g in 1 BOTTLE; Type 0: Not a Combination Product 12/15/2011 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 12/15/2011 Labeler - CINTEX SERVICES, LLC (078304114)
