PURELL SF607 INSTANT HAND SANITIZING- benzalkonium chloride liquid

Země: Spojené státy

Jazyk: angličtina

Zdroj: NLM (National Library of Medicine)

Aktivní složka:

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

Dostupné s:

GOJO Industries, Inc.

Podání:

TOPICAL

Druh předpisu:

OTC DRUG

Terapeutické indikace:

Antimicrobial - Hand sanitizer to help reduce bacteria on the skin

Stav Autorizace:

OTC monograph not final

Charakteristika produktu

PURELL SF607 INSTANT HAND SANITIZING- BENZALKONIUM CHLORIDE LIQUID
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 SF607 INSTANT HAND SANITIZING FOAM
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
Place enough product in your palm to thoroughly cover your hands
Rub hands together briskly until dry
Children under 6 years of age should be supervised when using this
product.
Water (Aqua), Decyl Glucoside, Glycerin, Methylparaben,
Phenoxyethanol, Propylparaben
PURELL SF607 INSTANT HAND SANITIZING
benzalkonium chloride liquid
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:21749-607
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)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLPARABEN (UNII: A2I8C7HI9T)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PACKAGING
# ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:21749-
607-31
45 mL in 1 BOTTLE; Type 0: Not a Combination
Product
01/03/2011
01/01/2024
GOJO Industries, Inc.
2
NDC:21749-
607-53
535 mL in 1 BOTTLE; Type 0: Not a Combination
Product
01/03/2011
01/01/2024
3
NDC:21749-
607-89
1200 mL in 1 BOTTLE; Type 0: Not a Combination
Product
01/03/2011
MARKETING INFORMATION
MARKETING
CATEGORY
APPLICATION NUMBER OR MONO