JEKSUNG

Manufacturer
Zhejiang Shiao Technology Co., Ltd.
Effective date
2020-04-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:35:32

Label at a glance#

ProductJEKSUNG
Active ingredientBENZETHONIUM CHLORIDE, QUATERNIUM-16, CLOTRIMAZOLE
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

30ML, 3-5 sprays each time, twice a day

WARNINGS SECTION

For external use only, Do not swallow When using this product
Keep out of eyes, ears, and mouth. If contact occurs, rinse with plenty of cold water right away and contact a physician. If swallowing, drink plenty of water and contact a physician
Please consult a doctor, if you have serious wounds, severe burns or animal bites.
Do not use this product if you are allergic to it.

INACTIVE INGREDIENT SECTION

WATER
METHANOL
ISOPROPYL ALCOHOL
N,N-DIMETHYLOCTADECYL AMINE
PROPYLENE GLYCOL, (S)-
PROPYLENE CARBONATE

OTC - ACTIVE INGREDIENT SECTION

CLOTRIMAZOLE
BENZETHONIUM CHL ORIDE
QUATERNIUM-16

INDICATIONS & USAGE SECTION

Hold the spray bottle (do not turn it upside down) withthe spray nozzle 10- 15cm away from the surface of the infectedarea, andspray evenly as far as possible, 3-5 sprays each time, twice a day, andspray on contacting object (if any)once a day. Each dose can be increased or decreased according to the actual situation of the patient. In severe cases, 10-15 sprays are recommended until the acute inflammation or major symptoms disappear.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

OTC - PURPOSE SECTION

This product can be used for anti-inflammatory debridement of wounds, and treatment of hair folliculitis, pustule sores, and jock itches caused by bacterial infection. It can also cooperate to treat beriberi, and cut off the source of infection by spraying on shoes and socks.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55451-00255451-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
a3b86cbb-eb52-8c74-e053-2995a90a9769a2c023e1-01ee-a631-e053-2a95a90aaa032020-04-20WarningsExact identifier
spl set id: a2c023e1-01ee-a631-e053-2a95a90aaa03

Reported adverse events (FAERS/openFDA)#

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