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- first aid 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.

JEKSUNG 
first aid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55451-002
Route of Administration	EXTRACORPOREAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.06 mg  in 30 mL
QUATERNIUM-16 (UNII: K4H0FG9I2T) (QUATERNIUM-16 - UNII:K4H0FG9I2T)	QUATERNIUM-16	0.06 mg  in 30 mL
CLOTRIMAZOLE (UNII: G07GZ97H65) (CLOTRIMAZOLE - UNII:G07GZ97H65)	CLOTRIMAZOLE	0.06 mg  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
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
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55451-002-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		01/21/2020	04/20/2020

Labeler - Zhejiang Shiao Technology Co., Ltd. (554518353)

Establishment
Name	Address	ID/FEI	Business Operations
Zhejiang Shiao Technology Co., Ltd.		554518353	manufacture(55451-002)

Revised: 4/2020

Document Id: a3b86cbb-eb52-8c74-e053-2995a90a9769

34390-5

Set id: a2c023e1-01ee-a631-e053-2a95a90aaa03

Version: 2

Effective Time: 20200420

 

Zhejiang Shiao Technology Co., Ltd.