GERM FREE DISINFECTANT GEL- hand sanitizer gel

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)

Available from:

Guangzhou Mengfeishi Pharmaceutical Technology Co., Ltd.

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

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

Authorization status:

OTC monograph not final

Summary of Product characteristics

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)
PURPOS E
Antibacterial sterilization
US E
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.
QUES TIONS ?
[phone]
PACKAGE LABEL - PRINCIPAL DISPLAY PANEL
GERM FREE DISINFECTANT GEL
hand sanitizer gel
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:77311-0 16
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
ALCO HO L (UNII: 3K9 9 58 V9 0 M) (ALCOHOL - UNII:3K9 9 58 V9 0 M)
ALCOHOL
70 mL in 10 0 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WATER (UNII: 0 59 QF0 KO0 R)
PRO PANEDIO L (UNII: 59 6 5N8 W8 5T)
CARBO MER HO MO PO LYMER, UNSPECIFIED TYPE (UNII: 0 A5MM30 7FC)
TRO LAMINE (UNII: 9 O3K9 3S3TK)
CHLO RPHENESIN (UNII: I6 70 DAL4SZ)
ALO E VERA LEAF (UNII: ZY8 1Z8 3H0 X)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKET