YESUL ANTIBACTERIAL HAND SANITIZER- alcohol gel

YESUL ANTIBACTERIAL HAND SANITIZER by

Drug Labeling and Warnings

YESUL ANTIBACTERIAL HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by N Bridge Inc., WHITE COSPHARM CO.,LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Alcohol

INACTIVE INGREDIENT

water, carbomer, polysorbate 20, isopropyl myristate, aminomethyl propanol, disodium edta, grapefruit extract, aloe vera gel

PURPOSE

Antiseptic

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

wet hands thoroughly with product and allow to dry without wiping

for children under 6, use only under adult supervision

not recommended for infants

WARNINGS

For external use only. Flammable. Keep away from heat or flame.

Do not use

• in children less than 2 months of age
• on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse thoroughly with water.

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.

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

YESUL ANTIBACTERIAL HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76966-0009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	350 mL  in 500 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GRAPEFRUIT (UNII: O82C39RR8C)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
WATER (UNII: 059QF0KO0R)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76966-0009-1	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/13/2020

Labeler - N Bridge Inc. (694892752)

Registrant - N Bridge Inc. (694892752)

Establishment
Name	Address	ID/FEI	Business Operations
WHITE COSPHARM CO.,LTD.		688442259	manufacture(76966-0009)

Establishment
Name	Address	ID/FEI	Business Operations
N Bridge Inc.		694892752	label(76966-0009)