![KAISER PERMANENTE BENZOYL PEROXIDE (BENZOYL PEROXIDE) SUSPENSION [KAISER FOUNDATION HOSPITALS]](https://medic.hrt.org//dailymed/images/5bd81128-0800-4d65-ba75-09cf6d7d5854/163KA-benzoyl-peroxide.jpg)
| NDC | 0179-8704-05 |
| Set ID | 5bd81128-0800-4d65-ba75-09cf6d7d5854 |
| Category | HUMAN OTC DRUG LABEL |
| Packager | Kaiser Foundation Hospitals |
| Generic Name | |
| Product Class | |
| Product Number | |
| Application Number | PART333D |
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only
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.
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Directions
- shake well
- Sensitivity Test for a New User. Apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs, follow the directions stated below.
- wet area to be cleansed
- apply acne wash and gently massage area for 1-2 minutes
- rinse thoroughly and pat dry
- 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.
- Inactive ingredients
- Questions or comments?
- Package/Label Principal Display Panel
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INGREDIENTS AND APPEARANCE
KAISER PERMANENTE BENZOYL PEROXIDE
benzoyl peroxide suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0179-8704 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE 10 g in 100 g Inactive Ingredients Ingredient Name Strength CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERIN (UNII: PDC6A3C0OX) IMIDUREA (UNII: M629807ATL) LAURYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EX0F4CZ66H) WATER (UNII: 059QF0KO0R) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0179-8704-05 142 g in 1 BOTTLE; Type 0: Not a Combination Product 06/08/2007 01/31/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 06/08/2007 01/31/2020 Labeler - Kaiser Foundation Hospitals (053052619)
