ANTIBACTERIAL HAND GEL- alcohol gel
Foshan MUZAR Cosmetics Co., Ltd

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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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.

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.

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

50 mL label 100 mL label 200 mL label 300 mL label 500 mL label

ANTIBACTERIAL HAND GEL
alcohol gel

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

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

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

#	Item Code	Package Description	Marketing Start Date
Packaging
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 Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	03/31/2020

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

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

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