REFRESH ANTIBAC FOAM- benzalkonium chloride soap

Страна: США

мова: англійська

Джерело: NLM (National Library of Medicine)

Активний інгредієнт:

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

Доступна з:

SC Johnson Professional USA, Inc.

ІПН (Міжнародна Ім'я):

BENZALKONIUM CHLORIDE

Склад:

BENZALKONIUM CHLORIDE 0.13 g in 1 L

Адміністрація маршрут:

TOPICAL

Тип рецепту:

OTC DRUG

Терапевтичні свідчення:

Antimicrobial for handwashing to reduce bacteria on the skin

Статус Авторизація:

OTC monograph not final

Характеристики продукта

REFRESH ANTIBAC FOAM- BENZALKONIUM CHLORIDE SOAP
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
BENZALKONIUM CHLORIDE, 0.13%
PURPOSE
Antimicrobial
USES
for handwashing to reduce bacteria on the skin
WARNINGS
FOR EXTERNAL USE ONLY
WHEN USING THIS PRODUCT
avoid contact with eyes. In case of eye contact, flush with water.
STOP USE AND ASK A DOCTOR IF
irritation and redness develop and persist for more than 3 days.
KEEP OUT OF REACH OF CHILDREN.
If swallowed, get medical help or contact a Poison Control Center
right away.
DIRECTIONS
apply foaming cleanser to dry hands
rub hands together to spread lather
wash for 15-20 seconds
rinse & dry hands thoroughly
INACTIVE INGREDIENTS
AQUA (WATER), GLYCERIN, LAURAMINE OXIDE, BUTYLENE GLYCOL, LACTIC ACID,
SALICYLIC ACID, PARFUM (FRAGRANCE), GREEN 5 (CI 61570), YELLOW 5 (CI
19140).
PRINCIPAL DISPLAY PANEL - 1 L BOTTLE LABEL
SCJ Professional
A family company
NDC 11084-010-66
Refresh™
ANTIBAC FOAM
Citrus Scent Antimicrobial Foam Handwash
Manufactured for: SC Johnson Professional USA, Inc.
Charlotte, NC 28217
1-800-248-7190 www.scjp.com
CITRUS FRAGRANCE
deb
SKIN CARE
1 L
(33.8 fl oz)
Made in Canada
L-1467 R0
®
REFRESH ANTIBAC FOAM
benzalkonium chloride soap
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:11084-010
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 g
in 1 L
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
SALICYLIC ACID (UNII: O414PZ4LPZ)
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)
FD&C YELLOW NO