NESURA INSTANT HAND SANITIZER- alcohol gel

Nesura Instant Hand Sanitizer by

Drug Labeling and Warnings

Nesura Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by CELLAB CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: Ethyl alcohol 70%

INACTIVE INGREDIENT

Inactive ingredients:

Water, Glycerin, Carbomer, Aloe Barbadensis Leaf Juice, Aminomethyl Propanol, Parfum, Citric Acid, Potassium Sorbate, Sodium Benzoate

PURPOSE

Purpose: antiseptic

WARNINGS

Warnings:

For external use only

Flammable, keep away from fire or 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 consult a doctor if
■ irritation and redness occur ■ condition persists for more than 72 hours

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

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:

■instant healthcare personnel hand antiseptic to reduce bacteria that potentially can cause disease

Directions

Directions:

■ Take an appropriate amount on your hands and rub thoroughly to dry.

Other Information

Other Information
- read the directions and warnings before use
- avoid freezing and excessive heat above 40 degree C (104 degree F)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NESURA INSTANT HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 57557-110
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	210 g  in 300 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
Potassium Sorbate (UNII: 1VPU26JZZ4)
Sodium Benzoate (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 57557-110-01	300 mL in 1 CONTAINER; 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 - CELLAB CO., LTD. (688195494)

Registrant - CELLAB CO., LTD. (688195494)

Establishment
Name	Address	ID/FEI	Business Operations
CELLAB CO., LTD.		688195494	manufacture(57557-110)