VIACHS FOLLICULITIS TREATMENT Cream
- Product NDC
- 84558-033
- 11-digit product format
- 845580033
- Labeler code
- 84558
- Product ID
- 84558-033_5be1dec8-f3e4-2f00-e063-6294a90a1717
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- VIACHS FOLLICULITIS TREATMENT Cream
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-08-20
- Substance
- BENZOYL PEROXIDE
- Active strength
- 5 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
- VIACHS FOLLICULITIS TREATMENT Cream
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZOYL PEROXIDE | 5 g/100g |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84558-033-01 | 84558003301 | 120 g in 1 BOTTLE (84558-033-01) | 120 g | 2026-09-18 | No | No | Current |