INSTANT HAND SANITIZER gel

Instant Hand Sanitizer by

Drug Labeling and Warnings

Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Xi'an Explution Tech Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Alcohol 80%v/v.

Purpose

Antimicrobial

USE

Hand Sanitizer to help reduce bacteria on skin.

WARNINGS

For external use only.

Flammable.Keep away from heat or flame.

DO NOT USE

When using this product

do not use on open skin Wounds.Keep out of eyes.ln.case of contact with eyes.rinse eyes thoroughly with water.

Use with caution if allergic to alcohoL.

STOP USE

Stop use and ask a doctor if irritation of rash appears and tasts.

Keep out of reach for children

If swallowed.get medical help or contact a Poison Control Center right away.

DIRECTIONS

1.Pump enough amount of product in your palm to thoroughly spread on both hands.

2.Rub thoroughly over all surfaces of both hands.

3.Rub hands together briskly until dry.

OTHER INFORMATION

Store below 106°F.(41°C)

May discolor certain fabrics or surface.

INACTIVE INGREDIENTS

glycerin.hydrogen peroxide, purified water.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

INSTANT HAND SANITIZER 
instant hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75709-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75709-002-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/30/2020
2	NDC: 75709-002-02	70 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/30/2020
3	NDC: 75709-002-03	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/30/2020
4	NDC: 75709-002-04	150 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/30/2020
5	NDC: 75709-002-05	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/30/2020
6	NDC: 75709-002-06	520 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/30/2020

Labeler - Xi'an Explution Tech Co.,Ltd. (554529088)

Registrant - Xi'an Explution Tech Co.,Ltd. (554529088)

Establishment
Name	Address	ID/FEI	Business Operations
Xi'an Explution Tech Co.,Ltd.		554529088	manufacture(75709-002)