XTREME HAND SANITIZER GEL 01- alcohol liquid

Xtreme Hand Sanitizer Gel by

Drug Labeling and Warnings

Xtreme Hand Sanitizer Gel by is a Otc medication manufactured, distributed, or labeled by Zhejiang Meizhiyuan Cosmetics Co., Ltd, Townley Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug facts

Kills 99.9% of germs

Active ingredient

Medicical Ingredient Purpose

Ethyl Alcohol 70-75% Antimicrobial

use

Hand sanitizer to help reduce bacterial on skin.

Wet hands thoroughly with product and rub the into skin.

warnings

For External Use Only.

Flammable: Keep away from flames.

Keep out of eyes. In case of contact with eyes, rinse eyes thoroughly with water.

Avoid contact with broken skin.

Do not inhale of ingest.

Stop use and contact a doctor if irritation develops or persists for more than 72 hours.

Keep out of reach of children.

If swallowed get immediate medical help or contact a poison contaol center right away.

Directions

Apply onto hands/skin, rub until dry.

Non-Medicinal

Water( aqua), Glycerin, propylene glycol, triethanolamine, carbomer, Aloe Barbadensis( Aloe Vera) gel, tocopheryl acetate( vitamin E)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

XTREME HAND SANITIZER GEL  01
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54304-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 100 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)	0.5 mL  in 100 mL
TROLAMINE (UNII: 9O3K93S3TK)	0.3 mL  in 100 mL
CARBOMER 940 (UNII: 4Q93RCW27E)	0.3 mL  in 100 mL
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)	0.05 mL  in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.05 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	28.3 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54304-020-01	60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/03/2020
2	NDC: 54304-020-02	237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/03/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/03/2020

Labeler - Zhejiang Meizhiyuan Cosmetics Co., Ltd (543036597)

Registrant - Townley Inc. (016956158)

Establishment
Name	Address	ID/FEI	Business Operations
Zhejiang Meizhiyuan Cosmetics Co., Ltd		543036597	manufacture(54304-020)