MULTI PURPOSE STERILIZATION HAND SANITIZER- alcohol spray

Multi purpose sterilization hand sanitizer by

Drug Labeling and Warnings

Multi purpose sterilization hand sanitizer by is a Otc medication manufactured, distributed, or labeled by GL Pharm. Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: Ethyl alcohol 83.0% v/v

INACTIVE INGREDIENT

Inactive ingredients:

Water

PURPOSE

Purpose: ANTISEPTIC

WARNINGS

Warnings:

For external use only-hands

Flammable. Keep away from heat and flame.

When using this product ■ Keep out of eyes. In case of contact with eyes,
flush thoroughly with water. ■ Avoid contact with broken skin. ■ Do not inhale
or ingest.

Stop use and ask a doctor if skin irritation or rash develops.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Uses

Uses:

■ Hand sanitizer to decrease bacteria on the skin that could cause disease
■ Disinfection of the skin at the surgical site

Directions

Directions:

■ Spray the product on skin or other place where disinfection is required.
■ Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

Other information
Store between 15-30C (59-86F)
Avoid freezing and excessive heat above 40C (104F)

Questions

Questions
http://www.glpharm.co.kr or TEL : +82-43-537-7001

Package Label : Multi-purpose sterilization hand sanitizer 100mL

Package Label : Multi-purpose sterilization hand sanitizer 300mL

Package Label : Multi-purpose sterilization hand sanitizer 350mL

INGREDIENTS AND APPEARANCE

MULTI PURPOSE STERILIZATION HAND SANITIZER 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74713-0500
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	83 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74713-0500-1	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/01/2020
2	NDC: 74713-0500-2	300 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/01/2020
3	NDC: 74713-0500-3	350 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/01/2020

Labeler - GL Pharm. Co., Ltd. (694506955)

Registrant - GL Pharm. Co., Ltd. (694506955)

Establishment
Name	Address	ID/FEI	Business Operations
GL Pharm. Co., Ltd.		694506955	manufacture(74713-0500)