PURELL HAND SANITIZING WIPES- benzalkonium chloride cloth

Страна: Соединенные Штаты

Язык: английский

Источник: NLM (National Library of Medicine)

Активный ингредиент:

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

Доступна с:

GOJO Industries, Inc.

Администрация маршрут:

TOPICAL

Тип рецепта:

OTC DRUG

Терапевтические показания :

Antimicrobial - Hand sanitizer to help reduce bacteria on the skin

Статус Авторизация:

OTC monograph not final

Характеристики продукта

PURELL HAND SANITIZING WIPES- BENZALKONIUM CHLORIDE 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
ACTIVE INGREDIENT
Benzalkonium Chloride 0.13%
PURPOSE
Antimicrobial
USES
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
benzalkonium chloride cloth
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:21749-368
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-
368-35
35 in 1 PACKAGE
03/14/2012
07/01/2022
1
150 mL in 1 PACKAGE; Type 0: Not a Combination
Product
2
NDC:21749-
368-10
100 in 1 PACKAGE
03/14/2012
2
245 mL in 1 PACKAGE; Type 0: Not a Combination
Product
3
NDC:21749-
368-27
270 in 1 PACKAGE
03/14/2012
3
667 mL in 1 PACKAGE; Type 0: Not a Combination
Product
4
NDC:21749-
368-12
1200 in 1 PACKAGE
03/14/2012
4
2567 mL in 1 PACKAGE; Type 0: Not a Combination
Product
5
NDC:217