PURELL HAND SANITIZING WIPES CLEAN REFRESHING SCENT- benzalkonium chloride wipe cloth

Χώρα: Ηνωμένες Πολιτείες

Γλώσσα: Αγγλικά

Πηγή: NLM (National Library of Medicine)

Δραστική ουσία:

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

Διαθέσιμο από:

GOJO Industries, Inc.

INN (Διεθνής Όνομα):

BENZALKONIUM CHLORIDE

Σύνθεση:

BENZALKONIUM CHLORIDE 0.00013

Οδός χορήγησης:

TOPICAL

Τρόπος διάθεσης:

OTC DRUG

Θεραπευτικές ενδείξεις:

Antimicrobial Hand sanitizer to help reduce bacteria on the skin

Καθεστώς αδειοδότησης:

OTC monograph not final

Αρχείο Π.Χ.Π.

PURELL HAND SANITIZING WIPES CLEAN REFRESHING SCENT- BENZALKONIUM
CHLORIDE WIPE CLOTH
GOJO INDUSTRIES, 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._
----------
PURELL HAND SANITIZING WIPES CLEAN REFRESHING SCENT
ACTIVE INGREDIENT
Benzalkonium Chloride 0.13%
ACTIVE INGREDIENT
Benzalkonium Chloride 0.13%
PURPOSE
Antimicrobial
USE
Hand sanitizer to help reduce bacteria on the skin
WARNINGS
FOR EXTERNAL USE ONLY
WHEN USING THIS PRODUCT do not use in or near the eyes. In case of
contact, rinse
eyes thoroughly with water.
STOP USE AND ASK A DOCTOR IF irritation or rash appears and lasts
KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or
contact a Poison
Control Center right away.
DIRECTIONS
• Wet hands thoroughly with product and allow to dry
• Children under 6 years of age should be supervised when using
PURELL
INACTIVE INGREDIENTS
Water (Aqua), Decyl Glucoside, Glycerin, Fragrance(Parfum),
Phenoxyethanol
PURELL HAND SANITIZING WIPES CLEAN REFRESHING SCENT
benzalkonium chloride wipe cloth
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:21749-359
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM -
UNII:7N6JUD5X6Y)
BENZ ALKONIUM
CHLORIDE
0.13 mg
in 100 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
WATER (UNII: 059QF0KO0R)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PACKAGING
# ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:21749-
359-10
10 in 1 PACKAGE
08/01/2014
1
37 mL in 1 PACKAGE; Type 0: Not a Combination
Product
2
NDC:21749-
359-15
15 in 1 PACKAGE
08/01/2014
02/02/2020
2
64 mL in 1 PACKAGE; Type 0: Not a Combination
Product
3
NDC:21749-
359-20
20 in 1 PACKAGE
08/01/2014
3
74 mL in 1 PACKAGE; Type 0: Not a Combinati