FIRST SAFETY HAND SANITIZING TISSUE- ethyl alcohol cloth

First safety hand sanitizing tissue by

Drug Labeling and Warnings

First safety hand sanitizing tissue by is a Otc medication manufactured, distributed, or labeled by BonitoLab Co., HANUL CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethy Alcohol 66% v/v

INACTIVE INGREDIENTS

Water, Glycerin, Citric Acid

PURPOSE

Antiseptic

WARNINGS

For external use only. Flammable. Keep away from heat or flame
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Do not use
■ on infants
■ on open skin wounds
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When using this product
■ avoid getting into the eyes
■ In case of eye contact immediately flush eyes thoroughly with water
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Stop use and ask a doctor
■ if irritation or redness develops
■ conditions persist for more than 72 hours
■ redness is present

KEEP OUT OF REACH OF CHILDREN

■ in case of accidental ingestion, contact a doctor or Poison Center immediately

Uses

■ hand sanitizing wipes to help reduce bacteria on the skin

Directions

■ Tear open packet, remove wipe
■ thoroughly wipes hands with cloth
■ Supervise children under 6 years of age when using this product

Other Information

■ Storage in a cool, dry place, Avoid freezing and excessive heat above 40 ℃ (104 ℉)
■ may discolor certain fabrics or surfaces

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FIRST SAFETY HAND SANITIZING TISSUE 
ethyl alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79984-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	Alcohol	66   in 100

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79984-010-01	30 in 1 CARTON; Type 0: Not a Combination Product	07/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/01/2020

Labeler - BonitoLab Co. (695505454)

Registrant - BonitoLab Co. (695505454)

Establishment
Name	Address	ID/FEI	Business Operations
HANUL CO.,LTD		557814370	manufacture(79984-010)