Face Acne Wash
- Product NDC
- 84365-008
- Requested package NDC
- 84365-008-01
- 11-digit product format
- 843650008
- Labeler code
- 84365
- Product ID
- 84365-008_5c05e56f-6a32-5412-e063-6394a90af7f1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzoyl Peroxide
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Shield Skin LLC
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-10-25
- Substance
- BENZOYL PEROXIDE
- Active strength
- 4 g/100mL
- 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
- Face Acne Wash
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| BENZOYL PEROXIDE | 4 g/100mL |
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 |
|---|---|---|---|---|---|---|---|
| 84365-008-01 | 84365000801 | 150 mL in 1 TUBE (84365-008-01) | 150 ml | 2026-10-25 | No | No | Current |