KEYSTONE- benzalkonium chloride solution

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)

Available from:

Ecolab Inc.

INN (International Name):

BENZALKONIUM CHLORIDE

Composition:

BENZALKONIUM CHLORIDE 0.1 mg in 100 mL

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

Antiseptic handwash - for handwashing to decrease bacteria on the skin

Authorization status:

OTC monograph not final

Summary of Product characteristics

KEYSTONE - BENZALKONIUM CHLORIDE SOLUTION
ECOLAB INC.
----------
DRUG FACTS
ACTIVE INGREDIENT
Benzalkonium chloride 0.1%
PURPOSE
Antiseptic handwash
USES
for handwashing to decrease bacteria on the skin
WARNINGS
FOR EXTERNAL USE ONLY
DO NOT USE
in eyes
WHEN USING THIS PRODUCT
discontinue use if irritation and redness develop
STOP USE AND ASK A DOCTOR IF
irritation and redness develop
KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or
contact a Poison
Control Center right away.
DIRECTIONS
wash hands to remove soil
dispense 20 mL into hand (palmful)
spread to cover hands, rub in well for at least 30 seconds
air dry, do not rinse or towel dry
OTHER INFORMATION
for additional information, see Safety Data Sheet (SDS)
for emergency medical information in USA and Canada, call
1-800-328-0026
for emergency medical information worldwide, call 1-651-222-5352 (in
the USA)
INACTIVE INGREDIENTS water (aqua), isopropyl alcohol, propylene
glycol, red 40, blue 1
QUESTIONS?
call 1-800-35-CLEAN (352-5326)
PRIMARY DISPLAY PANEL / REPRESENTATIVE LABEL
KEYSTONE SYSCO
FOAM HAND SANITIZER
Active Ingredient: Benzalkonium chloride 0.1%
SYSCO 7715473 6100098 ECOLAB
750 ML (25 US FL OZ)
DISTRIBUTED BY
SYSCO CORPORATION
Manufactured by:
Ecolab - 1 Ecolab Place - St. Paul MN 55102
tel: 1 800 35 CLEAN (352 5326)
(c) 2021 Ecolab USA Inc - All rights reserved
Made in U.S.A.
KEYSTONE
benzalkonium chloride solution
PRODUCT INFORMATION
Ecolab Inc.
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:47593-359
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM -
UNII:7N6JUD5X6Y)
BENZ ALKONIUM
CHLORIDE
0.1 mg
in 100 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
PACKAGING
# ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:47593-
359-41