CITRUS HAND SANITIZER- alcohol liquid

Maa: Yhdysvallat

Kieli: englanti

Lähde: NLM (National Library of Medicine)

Aktiivinen ainesosa:

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

Saatavilla:

Unique Holding Group Inc

Antoreitti:

TOPICAL

Prescription tyyppi:

OTC DRUG

Käyttöaiheet:

Stop using and ask a doctor if irritation or redness develops. Directions Put a thumb size amount in your palm and rub hands together briskly until dry.

Valtuutuksen tilan:

OTC monograph not final

Valmisteyhteenveto

CITRUS HAND SANITIZER - ALCOHOL LIQUID
UNIQUE HOLDING GROUP INC
_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._
----------
DRUG FACTS
ACTIVE INGREDIENT PURPOSE
Ethyl Alcohol 62% Sanitizer
US ES :
To decrease bacteria on the skin that could cause diseases
Recommended for repeated use
WARNINGS :
For external use only-hands. Use only as directed. Excessive use or
prolonged exposure may cause
irritation to skin. Discontinue use if rash, redness, or itching
occurs.
Flammable. Keep away from heat and flame. WHEN USING THIS PRODUCT
Keep out of eyes. In case of contacting with eyes, immediately flash
with water and call a doctor.
Avoid contacting with a broken skin.
STOP USING AND ASK A DOCTOR if irritation or redness develops.
KEEP OUT OF REACH OF CHILDREN.
In case of accidental ingestion, seek professional assistance or
contact a Poison Control Center
immediately.
DIRECTIONS
Put a thumb size amount in your palm and rub hands together briskly
until dry. OTHER INFORMATION
Do not store in temperatures over 118F
Children under six years of age should be supervise while using this
product.
May discolor certain fabrics.
INACTIVE INGREDIENTS
aloe barbadensis gel, carbomer, deionized water, FD and C Red No. 40,
FD and C Yellow No. 5,
Fragrance, glycerin, propylene glycol, triethanolamine, and vitamin E
labe
CITRUS HAND SANITIZER
alcohol liquid
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:25225-0 13(NDC:No ne )
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
6 2 g in 10 0 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WA TER (UNII: 0 59 QF0 KO0 R)
35.59 8 g in 10 0 g
PRO PYLENE GLYCO L (UNII: 6 DC9 Q16 7V3)
0 .5 g in 10 0 g
GLYCERIN (UNII: PDC6 A3C0 OX)
1 g in 10 0 g
ALO E VERA LEAF (UNII: ZY8 1Z8 3H0 X)
0