DERMASCO CLEAN AND FRESH HANDS SANITIZING- alcohol gel

DERMASCO Clean and Fresh Hands Sanitizing by

Drug Labeling and Warnings

DERMASCO Clean and Fresh Hands Sanitizing by is a Otc medication manufactured, distributed, or labeled by VAH CO., LTD, KOREA LIFE SCIENCE CO., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Alcohol (60%)

Uses

Hand sanitizer for decreasing bacteria on skin

Purpose

Antibacterial

Warnings

For external use only

Do not use if you are allergic to any of the ingredients

When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. avoid contact with broken, irritated, or itching skin. Do not puncture or incinerate.

Stop use and ask a doctor if irritation or redness develops and condition persists for more than 72 hours

If pregnant or breast-feeding, ask a health professional before use.

Directions

Take appropriate amount onto your hand and spread it all the way to fingertips. Rub the contents until it dries

Inactive ingredients

Water, Glycerin, Aminomethyl Propanol, Isopropyl Myristate, Carbomer, Tocopheryl Acetate, Propylene Glycol, Fragrance

Keep out of reach of children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

DERMASCO Hand Sanitizing GEL

INGREDIENTS AND APPEARANCE

DERMASCO CLEAN AND FRESH HANDS SANITIZING 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74187-100
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	30 g  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
GLYCERIN (UNII: PDC6A3C0OX)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74187-100-01	50 mL in 1 TUBE; Type 0: Not a Combination Product	04/02/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/02/2020

Labeler - VAH CO., LTD (695005295)

Establishment
Name	Address	ID/FEI	Business Operations
KOREA LIFE SCIENCE CO., LTD		694914835	manufacture(74187-100)