PRO-TEX HAND SANITIZER- hand sanitizer gel

Pro-Tex HAND SANITIZER by

Drug Labeling and Warnings

Pro-Tex HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Zhejiang Enchant Cosmetic Co., Ltd., GOODBUYS USA INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

75% Alcohol(V/V).

Purpose

Antibacterial and dialy hand cleaning.

Have antibacterial effect to staphylococcus aureus, escherichia coli, candida albicans.

Use

Squeeze out a small amount of formula properly and knead it with both hands.
Lasting for 1-3 minutes.

Warnings

Do not take the external product orally;
Do not touch the wound;
Do not contact the child directly;
If you contact the eyes carelessly, wash them with water in time;
Do not use this product instead of drugs;
Do not use it if you are allergic to alcohol.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Place enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

Keep away from sunlight and store in a cool and dry place.

Inactive ingredients

Water(Aqua), Carbomer, Aminomethyl propanol, Aloe Barbadensis Leaf Juice, Sodium Hyaluronate.

Package Label - Principal Display Panel

237 mL in 1 BOTTLE NDC: 52728-020-01

INGREDIENTS AND APPEARANCE

PRO-TEX HAND SANITIZER 
hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52728-020
Route of Administration	EXTRACORPOREAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	177.75 mL  in 237 mL

Inactive Ingredients
Ingredient Name	Strength
POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)	0.948 mL  in 237 mL
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)	0.711 mL  in 237 mL
WATER (UNII: 059QF0KO0R)	57.354 mL  in 237 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.2133 mL  in 237 mL
HYALURONATE SODIUM (UNII: YSE9PPT4TH)	0.0237 mL  in 237 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52728-020-01	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/10/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/10/2020

Labeler - Zhejiang Enchant Cosmetic Co., Ltd. (527284802)

Establishment
Name	Address	ID/FEI	Business Operations
GOODBUYS USA INC		041849319	label(52728-020)

Establishment
Name	Address	ID/FEI	Business Operations
Zhejiang Enchant Cosmetic Co., Ltd.		527284802	manufacture(52728-020)