Benzoyl Peroxide Acne Wash 5%
- Product NDC
- 58980-332
- 11-digit product format
- 589800332
- Labeler code
- 58980
- Product ID
- 58980-332_e35f3cd4-49a0-4881-9415-c6c325c7729c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzoyl Peroxide
- Dosage form
- SUSPENSION
- Route
- TOPICAL
- Labeler
- Stratus Pharmaceuticals
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-21
- Substance
- BENZOYL PEROXIDE
- Active strength
- 5 g/g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Benzoyl Peroxide Acne Wash 5%
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| BENZOYL PEROXIDE | 5 g/g |
openFDA label cross-check#
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.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 58980-332-50 | 58980033250 | 1 TUBE in 1 BOX (58980-332-50) / 141.8 g in 1 TUBE | 1 tube | 2026-10-01 | No | No | Current |
| 58980-332-80 | 58980033280 | 1 TUBE in 1 BOX (58980-332-80) / 226.8 g in 1 TUBE | 1 tube | 2026-10-01 | No | No | Current |