84558-033

Manufacturer
GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd
Effective date
2026-09-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-09-22 03:01:17

Label at a glance#

ProductVIACHS FOLLICULITIS TREATMENT Cream
Active ingredientBENZOYL PEROXIDE
Label structure12 sections

Dosage and administration

▪ Clean the affected area thoroughly and pat dry before application ▪ Apply a thin, even layer to affected skin 1 to 2 times daily ▪ If excessive dryness or irritation occurs,reduce to once daily or every other day tobuild skin tolerance ▪ For best results, use consistently as part of a daily body care routine ▪ Children under 12 years of age: consult adoctor before use

Storage and handling

▪ Store at 20" to 25°C (68° to 77°F) ▪ - Do not freeze ▪ - Keep tube tightly closed when not in use

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzoyl peroxide 5%

Purpose

OTC - PURPOSE SECTION

Topical antibacterial

Use

INDICATIONS & USAGE SECTION

· Treats and helps clear mild folliculitis and acne vulgaris (pimples, whiteheads, and blackheads)
· Penetrates hair follicles and pores to reduce follicle-associated bacteria
· Reduces redness and inflammation caused by follicular bumps
· Helps prevent new blemishes and follicular irritation from forming

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

· if you have very sensitive skin
· if you are allergic/sensitive to benzoyl peroxide

OTC - WHEN USING SECTION

▪ avoid contact with eyes, lips, mouth and mucous membranes. If contact occurs, rinse thoroughly with water.
▪ avoid contact with hair and dyed/colored fabrics, bedding and towels - this product may cause bleaching.
▪ skin irritation and dryness are more likely to occur if you use another topical acne medication at the same time. If irritation
occurs, only use one topical acne medication at a time.
▪ reduce application frequency if mild redness, itching or peeling occurs.
▪ limit sun exposure and use sunscreen on treated areas, as skin may become more sensitive to sunlight.▪

OTC - STOP USE SECTION

▪ severe skin irritation occurs (intenderness, burning, swelling or blistering)
▪ symptoms show no improvement after 4 weeks of consistent use
▪ the condition worsens

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.If swallowed, get
medical help or contact a Poison Control Center
immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

▪ Clean the affected area thoroughly and pat dry before application
▪ Apply a thin, even layer to affected skin 1 to 2 times daily
▪ If excessive dryness or irritation occurs,reduce to once daily or every other day tobuild skin tolerance
▪ For best results, use consistently as part of a daily body care routine
▪ Children under 12 years of age: consult adoctor before use

Other information

STORAGE AND HANDLING SECTION

▪ Store at 20" to 25°C (68° to 77°F)
▪ - Do not freeze
▪ - Keep tube tightly closed when not in use

Inactive ingredients

INACTIVE INGREDIENT SECTION

AQUA, BIFIDA FERMENT FILTRATE GLYCERIN, CETYL ETHYLHEXANOATE.
BUTYLENE GLYCOL, CETEARYL ALCOHOL, CAPRYLIC/CAPRIC TRIGLYCER-
IDE, BUTYROSPERMUM PARKII (SHEA) BUTTER, PEG-100 STEARATE, AMMONIUM
POLYACRYLOYLDIMETHYL TAURATE, MENTHOLUM, PORTULACA OLERACEA
EXTRACT. PEG-60 HYDROGENATED CASTOR OIL, CHRYSANTHELLUM INDICUM
EXTRACT, XANTHAN GUM, PENTAERYTHRI- TYL TETRA-DI-t-BUTYL HYDROXY
DROCINNAMATE, DISODIUM EDTA, ALOE BARBADENSIS EXTRACT

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

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Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84558-03384558-033-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Source Document#

Source XML

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.

Matched openFDA labels page 3 of 10 · 199 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SPOTLESS Acne Clearing TreatmentBENZOYL PEROXIDERodan & Fields3d4ef4ce-9be3-436a-9f93-c01caa93d1a82026-02-04WarningsName fallback
generic name: BENZOYL PEROXIDE
SPOTLESS REGIMEN FOR ACNE, BLEMISHES AND BREAKOUTSBENZOYL PEROXIDERodan & Fields8b2c187d-4b66-4872-8243-4365ea2e8b592026-02-04WarningsName fallback
generic name: BENZOYL PEROXIDE
Acne TreatmentBENZOYL PEROXIDECVS Pharmacy, Inc.d9fbaeba-cebf-4d02-aa7d-3ee1d2fdc50c2026-02-02Warnings, Adverse reactionsName fallback
generic name: BENZOYL PEROXIDE
Acne TreatmentBENZOYL PEROXIDERite Aid Corporationa51b7668-1ba1-42cb-b804-4fdf766106952026-01-30Warnings, Adverse reactionsName fallback
generic name: BENZOYL PEROXIDE
ZITFREE ACNE TREATMENTBENZOYL PEROXIDENatureplex, LLC70c2e3fb-e643-467b-80fd-c40e3c3e95132026-01-29WarningsName fallback
generic name: BENZOYL PEROXIDE
MEDPURA Benzoyl Peroxide Aqueous Base, Acne Treatment GelBENZOYL PEROXIDEAkron Pharma Inc.b7d335d1-3022-4b28-913c-477152a7dad22026-01-23WarningsName fallback
generic name: BENZOYL PEROXIDE
BenzoAzeline 10BENZOYL PEROXIDENoon Aesthetics M.R. Ltd985efa19-bd91-45cd-a2a0-d71ec325e51c2026-01-16WarningsName fallback
generic name: BENZOYL PEROXIDE
BenzoAzeline 5BENZOYL PEROXIDENoon Aesthetics M.R. Ltd0db88619-a1be-46d0-b1e7-26253a8c50e52026-01-16WarningsName fallback
generic name: BENZOYL PEROXIDE
Benzoazeline ForteBENZOYL PEROXIDENoon Aesthetics M.R. Ltdeb8c6984-2531-44c0-9a5d-5d64070f04ae2026-01-15WarningsName fallback
generic name: BENZOYL PEROXIDE
MEDPURA Benzoyl PeroxideBENZOYL PEROXIDEAkron Pharma Inc.1b051efe-054b-42a0-915a-b87885bd3c542026-01-13WarningsName fallback
generic name: BENZOYL PEROXIDE
PanOxylBENZOYL PEROXIDECrown Laboratories1660f219-e789-91f1-e063-6294a90a76642026-01-12WarningsName fallback
generic name: BENZOYL PEROXIDE
PanOxylBENZOYL PEROXIDECrown Laboratoriesff09cbab-304b-4da9-e053-6394a90ae6002026-01-12WarningsName fallback
generic name: BENZOYL PEROXIDE
PanOxylBENZOYL PEROXIDECrown Laboratories7b301b94-3cc8-b05b-e053-2991aa0aa5612026-01-12WarningsName fallback
generic name: BENZOYL PEROXIDE
Proactiv plus Pore Targeting TreatmentBENZOYL PEROXIDEAlchemee, LLC12f2eeab-d258-4eb1-8fe2-784c51c2e4cc2026-01-07WarningsName fallback
generic name: BENZOYL PEROXIDE
Proactiv Emergency Blemish ReliefBENZOYL PEROXIDEAlchemee, LLC72bb45ca-3f68-47be-928e-755cc66419d92026-01-07WarningsName fallback
generic name: BENZOYL PEROXIDE
Proactiv Renewing CleanserBENZOYL PEROXIDEAlchemee, LLC85c22f3a-b6c5-44a2-959c-532c6456ec302026-01-07WarningsName fallback
generic name: BENZOYL PEROXIDE
Proactiv Repairing TreatmentBENZOYL PEROXIDEAlchemee, LLC9bbf6db0-ff80-44d2-b81b-40080ca46b922026-01-07WarningsName fallback
generic name: BENZOYL PEROXIDE
Proactivplus Skin Smoothing ExfoliatorBENZOYL PEROXIDEAlchemee, LLCb56b63d6-5635-4fd4-9517-8b08c3cbf9aa2026-01-07WarningsName fallback
generic name: BENZOYL PEROXIDE
Sofie Pavitt Face Reset Benzoyl Peroxide Acne Treatment MaskBENZOYL PEROXIDECosco International, Inc.6d7fd1ce-2155-4aa4-87c6-c6fc0c0d3f422026-01-01WarningsName fallback
generic name: BENZOYL PEROXIDE
Clarity Clear Skin Solutions Acne Spot TreatmentBENZOYL PEROXIDEMelaleuca, Inc.193667e8-3a4d-9270-e063-6294a90a1c262025-12-31WarningsName fallback
generic name: BENZOYL PEROXIDE

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.