GERM FREE DISINFECTANT GEL- hand sanitizer gel

Germ Free Disinfectant Gel by

Drug Labeling and Warnings

Germ Free Disinfectant Gel by is a Otc medication manufactured, distributed, or labeled by Guangzhou Mengfeishi Pharmaceutical Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethanol 70% (v/v)

Purpose

Antibacterial sterilization

Use

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 of flame

Do not use

In children less than 2 months of age

On open skin wounds

When using this product

Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

If irritation or rash occurs. These may be signs of asrtious condition.

Keep out of reach of children.

If swallowed, get medical help or contact a poison Control Center right away.

Directions

Take appropriate amount of this product, rub with both hands until dry, no need to wash by hand.

Other information

Store between 15-30C (59-86F)

Avoid freexing and excessive heat above 40C(104F)

Inactive ingredients

water, propanediol, carbomer, triethanolamine, chlorphenesin, aloe barbadensis leaf extract.

Questions?

+83 20 36632232

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

GERM FREE DISINFECTANT GEL 
hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77311-016
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPANEDIOL (UNII: 5965N8W85T)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)
CHLORPHENESIN (UNII: I670DAL4SZ)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77311-016-02	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/10/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/10/2020

Labeler - Guangzhou Mengfeishi Pharmaceutical Technology Co., Ltd. (402685342)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Mengfeishi Pharmaceutical Technology Co., Ltd.		402685342	manufacture(77311-016)