MOISTURIZING HAND SANITIZER GREEN TEA- ethyl alcohol gel

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

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

Available from:

Mirfeel Korea Co., Ltd

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

ANTISEPTIC ㆍto decrease bacteria on the skin that could cause disease ㆍrecommended for repeated use

Authorization status:

OTC monograph not final

Summary of Product characteristics

MOISTURIZING HAND SANITIZER GREEN TEA- ETHYL ALCOHOL GEL
MIRFEEL KOREA 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
Ethyl alcohol 70%
INACTIVE INGREDIENT
Aqua, Carbomer, Triethanolamine, Jasminum Officinale (Jasmine)
Extract, Prunus Mume Flower
Extract, Bellis Perennis (Daisy) Flower Extract,
Fragrance, Aloe Barbadensis Extract, Tocopheryl Acetate, CI 42090, CI
19140
PURPOSE
ANTISEPTIC
WARNINGS
For external use only : hands
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Flammable, keep away from fire or flame
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When using this product
keep out of eyes. In case of contact with eyes, flush thoroughly with
water.
avoid contact with broken skin
do not inhale or ingest
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Stop use and ask a doctor
irritation or redness develops
condition persists for more than 72 hours
KEEP OUT OF REACH OF CHILDREN
If swallowed, get medical help or contact a Poison Control Center
right away.
US ES
to decrease bacteria on the skin that could cause disease
recommended for repeated use
DIRECTIONS
wet hands thoroughly with product and allow to dry without wiping
for children under 6, use only under adult supervision
not recommended for infants
do not consume
OTHER INFORMATION
store below 110 (43 )
may discolor some fabrics
harmful to wood finishes and plastics
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
MOISTURIZING HAND SANITIZER GREEN TEA
ethyl alcohol gel
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:750 10 -0 30
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) (ALCO