JEKSUNG by Zhejiang Shiao Technology Co., Ltd.

JEKSUNG by

Drug Labeling and Warnings

JEKSUNG by is a Otc medication manufactured, distributed, or labeled by Zhejiang Shiao Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

JEKSUNG- anti-inflammatory antibacterial spray liquid 
Zhejiang Shiao Technology Co., Ltd.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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

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.

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

CLOTRIMAZOLE
BENZETHONIUM CHL ORIDE
QUATERNIUM-16

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.

KEEP OUT OF REACH OF CHILDREN

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.

outer-packaging

JEKSUNG 
anti-inflammatory antibacterial spray liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 55451-001
Route of AdministrationEXTRACORPOREAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE0.06 mg  in 30 mL
QUATERNIUM-16 (UNII: K4H0FG9I2T) (QUATERNIUM-16 - UNII:K4H0FG9I2T) QUATERNIUM-160.06 mg  in 30 mL
CLOTRIMAZOLE (UNII: G07GZ97H65) (CLOTRIMAZOLE - UNII:G07GZ97H65) CLOTRIMAZOLE0.06 mg  in 30 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
METHYL ALCOHOL (UNII: Y4S76JWI15)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
DYMANTHINE (UNII: 066975NG22)  
PROPYLENE GLYCOL, (S)- (UNII: 942194N4TD)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 55451-001-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product01/21/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other01/21/202004/21/2020
Labeler - Zhejiang Shiao Technology Co., Ltd. (554518353)
Establishment
NameAddressID/FEIBusiness Operations
Zhejiang Shiao Technology Co., Ltd.554518353manufacture(55451-001)

Revised: 4/2020
Document Id: a3db7558-5a9f-5016-e053-2995a90a1c31
Set id: 9d10a470-87fa-79bc-e053-2a95a90a4be8
Version: 2
Effective Time: 20200422