YI JIE NINGTM GEL ANTIBACTERIAL HAND SANITIZER- hand sanitizer gel

Yi Jie NingTM Gel Antibacterial Hand Sanitizer by

Drug Labeling and Warnings

Yi Jie NingTM Gel Antibacterial Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Weifang Sinnovation Medical Technology Co.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Alcohol 75%

Purpose

Antiseptic

Uses

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame.

Do not use

˙in children less than 2 months of age

˙on open skin wounds

WHEN USING

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

STOP USE

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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.

Directions

Apply an appropriate amount of this product to the skin surface of the hands (palm, back of the hands, between fingers) until moist, rub each other for 1-2 minutes to dry naturally.

Other Information

Sealed, stored in a cool, dry place

[Production Date]

[Product Lot Number]

[Valid Until]

Inactive Ingredients

Benzalkonium Bromide, Glycerin

Package Label

Yi Jie NingTM Gel Antibacterial Hand Sanitizer

Alcohol Antiseptic 75%

Topical Gel

Hand Sanitizer

Non-Sterile Gel

100ml / Bottle

NDC: 76879-001-01

INGREDIENTS AND APPEARANCE

YI JIE NINGTM GEL ANTIBACTERIAL HAND SANITIZER 
hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76879-001
Route of Administration	TOPICAL

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)	24.5 mL  in 100 mL
BENZALKONIUM BROMIDE (UNII: 151T1GQ42D)	0.5 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76879-001-01	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/01/2020

Labeler - Weifang Sinnovation Medical Technology Co.,Ltd (554531955)

Registrant - Weifang Sinnovation Medical Technology Co.,Ltd (554531955)

Establishment
Name	Address	ID/FEI	Business Operations
Weifang Sinnovation Medical Technology Co.,Ltd		554531955	manufacture(76879-001)