INSTANT HAND SANITIZER- 75% alcohol gel

Instant Hand Sanitizer by

Drug Labeling and Warnings

Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Zhejiang Yangxiang Technology Co., Ltd, A03 Lab of BTS. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

Hand sanitizer to help decrease bacteria skin.

Use

Hand sanitizer to help reduce bacteria on skin.

Warnings

Flammable, Keep away from fire or flame.
For external use only.

Do not use

When using this product do not use in or near the eyes.

In case of contact, rinse eyes thoroughly with water.

WHEN USING

When using this product do not use in or near the eyes.

In case of contact, rinse eyes thoroughly with water.

STOP USE

Stop using if skin allergles occurs.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

If swallowed, get medical help or contact poisions control center right away.

Directions

Put enough product on your palm to cover hands and rub hands together briskly until dry.

Children under 6 years of age should be supervised when using this product.

Other information

Store at a cool place, avoid sunlight.

Inactive ingredients

Aqua (water), Glycerin, Carbomer, Triethanolamine, Vitamin E extract.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

INSTANT HAND SANITIZER 
75% alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75589-101
Route of Administration	EXTRACORPOREAL

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
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)
.ALPHA.-TOCOPHEROL, D- (UNII: N9PR3490H9)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75589-101-25	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020
2	NDC: 75589-101-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020
3	NDC: 75589-101-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020
4	NDC: 75589-101-15	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/01/2020

Labeler - Zhejiang Yangxiang Technology Co., Ltd (554530914)

Registrant - A03 Lab of BTS (548009541)

Establishment
Name	Address	ID/FEI	Business Operations
Zhejiang Yangxiang Technology Co., Ltd		554530914	manufacture(75589-101) , label(75589-101)