84558-032

Manufacturer
GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd
Effective date
2026-09-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-09-16 01:00:52

Label at a glance#

ProductELOREVIA FOLLICULITIS TREATMENT Cream
Active ingredientBENZOYL PEROXIDE
Label structure12 sections

Dosage and administration

Clean the affected area. Apply a thin layer to the affected area. Apply once daily. If needed, increase to twice daily. lf bothersome dryness or peeling occurs, reduce application to once daily or every other day.

Storage and handling

store at 20°-25°C (68°-77°F), Close the cap tightly after 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

For the treatment of folliculitis
Helps reduce follicle bumps and pustules
Helps relieve redness and irritation

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

Have very sensitive skin
Are sensitive to benzoyl peroxide

OTC - WHEN USING SECTION

Avoid contact with eyes, lips, mouth, and mucousmembranes.
If contact occurs, rinse thoroughly with water.

Avoid contact with hair and dyed fabrics, which may be bleached.

OTC - STOP USE SECTION

Severe irritation or redness develops.
Condition worsens.
Symptoms persist for more than 7 days or clear up and occur again within a few days.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a
Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Clean the affected area.
Apply a thin layer to the affected area.
Apply once daily. If needed, increase to twice daily.
lf bothersome dryness or peeling occurs, reduce application to once daily or every other day.

Other information

STORAGE AND HANDLING SECTION

store at 20°-25°C (68°-77°F), Close the cap
tightly after use.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, C12-15 Alkyl Benzoate,
Propylene Glycol, Glyceryl Stearate, Cetearyl
Alcohol, Squalane, Aloe Barbadensis Leaf
Juice, Dimethicone, Hydroxyethy| Acrylate/
Sodium Acryloyldimethyl Taurate Copolyer,
Phenoxyethanol, Panthenol, PEG-100
Stearate, Polysorbate80, Magnesium
Aluminum Silicate, Ceramide NP,Sodium
Hydroxide, Allantoin, Scutellaria Baicalensis
Root Extract, Forsythia Suspensa Fruit Extract,
Portulaca Oleracea Extract, Magnolia Officinalis
Bark Extract, Calendula Officinalis Flower
Extract, Melaleuca Alternifolia(Tea Tree) Leaf
Oil, Menthyl Lactate, Ethylhexylglycerin,
Disodium EDTA.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84558-03284558-032-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-09-01daily-update2026-09-04 01:00:59

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
5a770e66-a414-ff45-e063-6394a90af02c5a770e5b-5bba-2213-e063-6294a90a32582026-09-01WarningsExact identifier
spl set id: 5a770e5b-5bba-2213-e063-6294a90a3258

Reported adverse events (FAERS/openFDA)#

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