CHUNG SOL DISINFECTION ETHANOL- ethyl alcohol spray 
Samhyun pharma

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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ACTIVE INGREDIENT

Ethanol 83% v/v

INACTIVE INGREDIENT

Purified water

PURPOSE

ANTISEPTIC

WARNINGS

For external use only.
■ Flammable, keep away from heat or flame
■ If taken, internally serious gastric disturbances will result
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Ask a doctor before use if you have
■ Deep or puncture wounds, animal bites or serious burns
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When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

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

Uses

■ To help prevent the risk of infection in minor cuts, scrapes and burns
■ To help reduce bacteria that can cause disease

Directions

■ Place enough products on hands to cover all surfaces.
■ Supervise children under 6years of age when using this product to avoid swallowing.

Other information

Keep away from heat / sparks / open flames / hot surfaces
■ Store between 15-30C (59-86F)
■ Avoid freezing and excessive heat above 40C (104F)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottle

CHUNG SOL DISINFECTION ETHANOL 
ethyl alcohol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75765-030
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL830 mL  in 1000 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:75765-030-011000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/01/2020
Labeler - Samhyun pharma (694185214)
Registrant - Samhyun pharma (694185214)
Establishment
NameAddressID/FEIBusiness Operations
Samhyun pharma694185214manufacture(75765-030)

Revised: 7/2020
Document Id: 8528bdee-f37d-4122-a8b7-27ac9f607338
Set id: df4faa86-f02f-4fbe-b470-da3e62dc676f
Version: 1
Effective Time: 20200720
 
Samhyun pharma