HANDS-FREE SURGICAL GEL gel

Hands-free Surgical Gel by

Drug Labeling and Warnings

Hands-free Surgical Gel by is a Otc medication manufactured, distributed, or labeled by Jiangxi Baiyi Weishi Medical Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

Closed and stored in a cool, ventilated and dry place

INACTIVE INGREDIENT

Purified water

INDICATIONS & USAGE

1. Disinfect external hands: Wash and dry your hands and forearms with soap solution, then take about 5min of thisproduct. Rub the hands and forearms evenly for 3 minutes according to the (disinfection technical specifications). Bacteria gloves.
2. Take 3ml of this product's original solution and rub it with your hands for 1 minute during inspection, treatment and nursing of
patients.
3. Sanitize your hands after daily work: Take about 3ml of this product and rub your hands for 1 minute.

ACTIVE INGREDIENT

Ethanol

n-propanol

KEEP OUT OF REACH OF CHILDREN

Ethanol 65%, n-propanol 9%

PURPOSE

Disinfection
Sterilization
No Rinseing

WARNINGS

1. Disinfectant for external use should not be taken orally
2. This product is used to clean dry hands
3. This product contains ethanol, which is iritating to damaged skin and mucous membranes. It is prohibited for those who are allergic to ethanol
4. Closed and stored in a cool, ventilated and dry place
5. Valid for 24 months

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HANDS-FREE SURGICAL GEL 
hands-free surgical gel gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 40796-003
Route of Administration	EXTRACORPOREAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	325 mL  in 500 mL
PROPYL ALCOHOL (UNII: 96F264O9SV) (PROPYL ALCOHOL - UNII:96F264O9SV)	PROPYL ALCOHOL	45 g  in 500 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code	economical
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 40796-003-01	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/13/2020

Labeler - Jiangxi Baiyi Weishi Medical Technology Co., Ltd. (407967698)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Baiyi Weishi Medical Technology Co., Ltd.		407967698	manufacture(40796-003)