ALCOHOL SANITIZING- alcohol sanitizing spray spray

Alcohol Sanitizing by

Drug Labeling and Warnings

Alcohol Sanitizing by is a Otc medication manufactured, distributed, or labeled by Guangzhou Joy Claire Biological Technology Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Ethyl Alcohol 72.5%-77.5%(VM)

Purpose

Antiseptic

Uses

Sanitizing for surfaces of hard objects in hospitals,homes and public areas, full skin surface,

surgeries, fabrics and other surfaces of porous objects.

WARNINGS

Flammable.Keep away from heat and flame

For external use， do not inhale or ingest.Keep out of reach of children.

Avoid contact with broken skin and keep out of eyes.In case of contact with eyes， flush

thoroughly with water.

Store below 43℃.Avoid lights and preserve in cool， dry and ventilated places.

This product contains ethyl alcohol.Please test on a small area of skin before use， and stop

use if skin imtaion develops

Shall not apply as sanitizing for metalware.

DO NOT USE

WHEN USING

STOP USE

KEEP OUT OF REACH OF CHILDREN

Directions

1.Sanitize on full skin surface：Put 3ml of this product where needs sanitized and leave acting

for 3 minutes

2.Put 5ml of this product on surfaces of clothing and leave for 2 minutes without rinse

3.Sanitize on object surfaces at home， school， public area and hospital：Put 5ml of this product

on the object surfaces need sanitized and leave acting for 2 minutes without rinse

4.Available for hand sanitizing at home， school public area and hospital Put 2ml of this product

in palm and rub hands together for 1 minute until dry.

5.Surgery：Cleanse hands and forearms with soap， when dry， put 2ml of this product under the

instruction of Regulation of Disinfection Technique， thoroughly rub hands and forearms for 3

minutes without rinse， then put on sterile gloves.

STORAGE AND HANDLING

INACTIVE INGREDIENT

Label

INGREDIENTS AND APPEARANCE

ALCOHOL SANITIZING 
alcohol sanitizing spray spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74743-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 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: 74743-001-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/08/2020
2	NDC: 74743-001-02	80 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/08/2020
3	NDC: 74743-001-03	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/08/2020
4	NDC: 74743-001-04	150 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/08/2020
5	NDC: 74743-001-05	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/08/2020

Labeler - Guangzhou Joy Claire Biological Technology Co., Ltd (418209894)

Registrant - Guangzhou Joy Claire Biological Technology Co., Ltd (418209894)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Joy Claire Biological Technology Co., Ltd		418209894	manufacture(74743-001)