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
Drug Label Information
Updated December 11, 2024
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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 Drug M006 12/15/2011 Labeler - CINTEX SERVICES, LLC (078304114)