BYT BANGYTONG 5% BENZOYL PEROXIDE FOLLICULITIS CREAM

Manufacturer
Shenzhen Jindali Technology Co., Ltd
Effective date
2026-08-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-21 02:01:47

Label at a glance#

ProductBYT BANGYTONG FOLLICULITIS
Active ingredientBENZOYL PEROXIDE
Label structure12 sections

Dosage and administration

Clean the skin thoroughly before applying. Apply a thin layer to affected areas 1 to 3 times daily. Start with once daily, gradually increase to 2-3 times if needed. If dryness or peeling occurs, reduce to once daily or every other day.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzoyl peroxide 5%

Purpose

INDICATIONS & USAGE SECTION

Topical antibacterial

Use

OTC - PURPOSE SECTION

Treats and helps clear mild folliculitis and acne vulgaris (pimples,
whiteheads, and blackheads) by penetrating pores to help reduce
acne-causing bacteria, reduce redness and inflammation, and help
prevent new blemishes.

Warnings

DOSAGE & ADMINISTRATION SECTION

For external use only.

Do not use

WARNINGS SECTION

Do not use if you are sensitive to benzoyl peroxide.

When Using

OTC - WHEN USING SECTION

.avoid unnecessary sun exposure and use a sunscreen.
.avoid contact with the eyes, lips, and mouth.
.avoid contact with hair and dyed fabrics, which may be bleached by this product.
.skin irritation may occur, characterized by redness, burning, itching,
peeling, or swelling. Reduce frequency of use if irritation occurs.

STOP USE

OTC - STOP USE SECTION

. irritation becomes severe.
. no improvement is seen after 6 weeks of consistent use.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact
Poison Control right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Clean the skin thoroughly before applying. Apply a thin layer to affected
areas 1 to 3 times daily. Start with once daily, gradually increase to 2-3
times if needed. If dryness or peeling occurs, reduce to once daily or
every other day.

Other information

OTHER SAFETY INFORMATION

Store at 20°-25°C(68°-77°F). Do not use if the carton or inner seal is broken.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, C12-15 Alkyl Benzoate, Propylene Glycol, Glyceryl
Stearate, Cetearyl Alcohol, Squalane, Aloe Barbadensis Leaf Juice,
Dimethicone, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate
Copolymer, Phenoxyethanol, Panthenol, PEG-100 Stearate,
Polysorbate 80, 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, Menthy| Lactate, Ethylhexylglycerin, Disodium EDTA

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

5% BENZOYL PEROXIDE FOLLICULITIS CREAM5% BENZOYL PEROXIDE FOLLICULITIS CREAM

Products#

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

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87382-02687382-026-01

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

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
BYT BANGYTONG FOLLICULITIS5% BENZOYL PEROXIDE FOLLICULITISShenzhen Jindali Technology Co., Ltd595363f9-6aee-93a5-e063-6394a90a0f0e2026-08-18WarningsExact identifier
ndc (package): 87382-026-01
ndc (product): 87382-026
ndc11 (package): 87382002601
spl id: 595363f9-6aef-93a5-e063-6394a90a0f0e
spl set id: 595363f9-6aee-93a5-e063-6394a90a0f0e

Reported adverse events (FAERS/openFDA)#

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