ANTIBACTERIAL HAND GEL- alcohol gel

Antibacterial Hand gel by

Drug Labeling and Warnings

Antibacterial Hand gel by is a Otc medication manufactured, distributed, or labeled by Foshan MUZAR Cosmetics Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Alcohol 50%

Purpose

Antimicrobial

Uses

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.Stop use and ask doctor if irritation or rash appears and lasts.Keep out of reach for children. if swallowed,get medical help or contact a With Vitamin E& Poison Control Center right away.

STOP USE

KEEP OUT OF REACH OF CHILDREN

Directions

Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry.

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

Other information

Store below 106° F.(41 ° C)

May discolor certain fabrics or surfaces

Inactive ingredients

Water,glycerin,cabo,alcohol,triethanolamine,940

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL HAND GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74041-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	50 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74041-001-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/31/2020
2	NDC: 74041-001-02	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/31/2020
3	NDC: 74041-001-03	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/31/2020
4	NDC: 74041-001-04	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/31/2020
5	NDC: 74041-001-05	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/31/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/31/2020

Labeler - Foshan MUZAR Cosmetics Co., Ltd (554526583)

Registrant - Foshan MUZAR Cosmetics Co., Ltd (554526583)

Establishment
Name	Address	ID/FEI	Business Operations
Foshan MUZAR Cosmetics Co., Ltd		554526583	manufacture(74041-001)