Cleanse the skin thoroughly before applying medication. Cover the entire affected area with a thin layer 1 to 3 times daily. Because excessive drying of the skin may occur, start with 1 application daily, then gradually increase to 2 or 3 times daily if needed or as directed by a doctor. If bothersome dryness or peeling occurs, reduce application use to once a day or every other day. If going outside, use a sunscr...
Drug Facts
Benzoyl Peroxide 2.5%
Acne Treatment
For the management of acne
For external use only
Do not use this medication if you have very sensitive skin or if you are sensitive to benzoyl peroxide.
Ask a doctor or pharmacist before use if you are using other topical acne medications at the same time or immediately following use of this product. This may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.
Stop use and ask a doctor if skin irritation occurs.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
water (aqua), ethoxydiglycol, cyclotetrasiloxane, propylene glycol, cetearyl alcohol, dimethicone, glyceryl stearate, PEG-100 stearate, cyclopentasiloxane, panthenol, allantoin, xanthan gum, ceteareth-20, carbomer, triethanolamine, diazolidinyl urea, methylparaben, propylparaben, fragrance (parfum)
Combination Therapy®
3
2 FL. OZ. 60 mL
benzoyl peroxide acne treatment
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Benzoyl Peroxide | ACTIVE INGREDIENT | W9WZN9A0GM | 1 | |
| Benzoyl Peroxide | ACTIVE MOIETY | W9WZN9A0GM | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 11410-207 | 11410-207-35, 11410-207-20, 11410-207-23, 11410-207-10 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Benzoyl Peroxide | W9WZN9A0GM | ACTIB |
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 34b46efa-9e1c-4f50-a255-9342f713d640 | 983be8a4-0ebb-4cb7-bcb0-3396b44ee060 | 2010-05-07 | Warnings | 34b46efa-9e1c-4f50-a255-9342f713d640 983be8a4-0ebb-4cb7-bcb0-3396b44ee060 |
Adverse event summaries are temporarily unavailable. Other product information remains available.