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
IngredientStrength
BENZOYL PEROXIDE5 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
W9WZN9A0GMInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
308693Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
5bb87e5b-e41a-bea7-e063-6394a90ae7afAvailable on FDA.report

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
84558-033-0184558003301120 g in 1 BOTTLE (84558-033-01) 120 g2026-09-18NoNoCurrent