FOLLICULITIS Cream
- Product NDC
- 84558-034
- 11-digit product format
- 845580034
- Labeler code
- 84558
- Product ID
- 84558-034_5caa5f35-2110-6851-e063-6394a90afbf6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- FOLLICULITIS Cream
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-08-20
- Substance
- BENZOYL PEROXIDE
- Active strength
- 10 g/100g
- 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
- FOLLICULITIS Cream
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| BENZOYL PEROXIDE | 10 g/100g |
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 |
|---|---|---|---|---|---|---|---|
| 84558-034-01 | 84558003401 | 120 g in 1 BOTTLE (84558-034-01) | 120 g | 2026-09-30 | No | No | Current |