Label: BP WASH- benzoyl peroxide emulsion
- NDC Code(s): 24470-901-05, 24470-901-08
- Packager: CINTEX SERVICES, LLC
- Category: HUMAN OTC DRUG LABEL
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.
Updated December 22, 2020
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Active ingredient
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
- 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
- PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
benzoyl peroxide emulsion
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:24470-901 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE 100 mg in 1 g Inactive Ingredients Ingredient Name Strength COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) MINERAL OIL (UNII: T5L8T28FGP) POLYETHYLENE OXIDE 600000 (UNII: 2126FD486L) HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY) WATER (UNII: 059QF0KO0R) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) IMIDUREA (UNII: M629807ATL) SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493) STARCH, CORN (UNII: O8232NY3SJ) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) DIMETHYL ISOSORBIDE (UNII: SA6A6V432S) METHYLPARABEN (UNII: A2I8C7HI9T) SALICYLIC ACID (UNII: O414PZ4LPZ) SODIUM HYDROXIDE (UNII: 55X04QC32I) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:24470-901-05 142 g in 1 BOTTLE; Type 0: Not a Combination Product 01/15/2012 2 NDC:24470-901-08 227 g in 1 BOTTLE; Type 0: Not a Combination Product 01/15/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 01/15/2012 Labeler - CINTEX SERVICES, LLC (078304114)