GERM FREE DISINFECTANT GEL- hand sanitizer gel 
Guangzhou Mengfeishi Pharmaceutical Technology 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

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

77311-016

GERM FREE DISINFECTANT GEL 
hand sanitizer gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77311-016
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:77311-016-02500 mL in 1 BOTTLE; Type 0: Not a Combination Product06/10/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/10/2020
Labeler - Guangzhou Mengfeishi Pharmaceutical Technology Co., Ltd. (402685342)
Establishment
NameAddressID/FEIBusiness Operations
Guangzhou Mengfeishi Pharmaceutical Technology Co., Ltd.402685342manufacture(77311-016)

Revised: 5/2020
Document Id: a614ad37-90c7-20a5-e053-2995a90a6f1c
Set id: a614ad37-90c6-20a5-e053-2995a90a6f1c
Version: 1
Effective Time: 20200521
 
Guangzhou Mengfeishi Pharmaceutical Technology Co., Ltd.