CLEAN CHOICE ALCOHOL SANITIZER- ethyl alcohol liquid

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

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

Available from:

SC Johnson Professional USA, Inc.

INN (International Name):

ALCOHOL

Composition:

ALCOHOL 70 L in 100 L

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

Antibacterial for hand sanitizing to reduce bacteria on the skin

Authorization status:

OTC monograph not final

Summary of Product characteristics

CLEAN CHOICE ALCOHOL SANITIZER- ETHYL ALCOHOL LIQUID
SC JOHNSON PROFESSIONAL USA, 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
ETHYL ALCOHOL 70% w/w
PURPOS E
Antibacterial
US ES
for hand sanitizing to reduce bacteria on the skin
WARNINGS
For external use only
FLAMMABLE.
Keep away from fire or flame.
WHEN USING THIS PRODUCT
avoid contact with eyes. In case of eye contact, flush with water.
KEEP OUT OF REACH OF CHILDREN.
If swallowed, get medical help or contact a Poison Control Center
right away.
DIRECTIONS
apply foaming sanitizer to cover hands
rub into skin
no rinsing required
INACTIVE INGREDIENTS
AQUA (WATER), BEHENTRIMONIUM CHLORIDE, BIS-PEG-12 DIMETHICONE, COCO-
GLUCOSIDE, DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE, GLYCERYL
OLEATE, PEG-200 HYDROGENATED GLYCERYL PALMATE, PEG-7 GLYCERYL COCOATE.
Clean Choice
NDC 11084-704-12
Foaming Alcohol Hand Sanitizer
UL ECOLOGO
PRODUCTS CERTIFIED FOR REDUCED ENVIRONMENTAL IMPACT. VIEW
SPECIFIC ATTRIBUTES EVALUATED: UL.COM/EL
UL 2783
1 L (33.8 fl oz)
Stock # 0617388
DCN9254/0517
L-1417 R0
Distributed Exclusively by Fastenal
Distributed by Fastenal Company and its Subsidiaries
Winona, MN 55987
(C)2017 fastenal.com
Made in Canada
CLEAN CHOICE ALCOHOL SANITIZER
ethyl alcohol liquid
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:110 8 4-70 4
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 L in 10 0 L
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WATER (UNII: 0 59 QF0 KO0 R)
BEHENTRIMO NIUM CHLO RIDE (UNII: X7GNG3S47T)
BIS-PEG-12 DIMETHICO NE ( 50 0 MPA.S) (UNII: 2CNS542YRT)
CO CO GLUCO SIDE (UNII: ICS79 0 225B)
DIHYDRO XYPRO PYL PEG-5 LINO LEAMMO NIUM CHLO RIDE (UNII: 0 Y0
NQR2GH1)
GLYCERYL O LEATE (UNII: