PIONEER ECLIPSE TOUCHE FOAMING NON-ALCOHOL HAND SANITIZER- benzalkonium chloride solution

Valsts: Amerikas Savienotās Valstis

Valoda: angļu

Klimata pārmaiņas: NLM (National Library of Medicine)

Nopērc to tagad

Produkta apraksts Produkta apraksts (SPC)
21-09-2023

Aktīvā sastāvdaļa:

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

Pieejams no:

CWGC LA Inc.

SNN (starptautisko nepatentēto nosaukumu):

BENZALKONIUM CHLORIDE

Kompozīcija:

BENZALKONIUM CHLORIDE 0.13 g in 100 mL

Ievadīšanas:

TOPICAL

Receptes veids:

OTC DRUG

Ārstēšanas norādes:

- For handwashing to reduce bacteria on the skin. Recommended for repeated use. Stop use and ask a doctor if irritation or redness develops and persists.

Autorizācija statuss:

OTC monograph not final

Produkta apraksts

                                PIONEER ECLIPSE TOUCHE FOAMING NON-ALCOHOL HAND SANITIZER-
BENZALKONIUM CHLORIDE SOLUTION
CWGC LA 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._
----------
CWGC - PIONEER ECLIPSE TOUCHÉ FOAMING NON-ALCOHOL HAND SANITIZER
(70415-
305)
ACTIVE INGREDIENT
BENZALKONIUM CHLORIDE 0.13%
PURPOSE
Antibacterial
_USES_
For handwashing to reduce bacteria on the skin. Recommended for
repeated use.
_WARNINGS_
FOR EXTERNAL USE ONLY
AVOID CONTACT WITH EYES. IN CASE OF EYE CONTACT, FLUSH EYES WITH
WATER.
Keep out of reach of children. If swallowed, get medical help or
contact a Poison Control
Center right away.
Stop use and ask a doctor if irritation or redness develops and
persists.
_DIRECTIONS_
Apply foam sanitizer to hands.
Rub over surfaces of both hands for 15 seconds.
No rinsing required.
_INACTIVE INGREDIENTS_
WATER, COCO-GLUCOSIDE, LAURTRIMONIUM CHLORIDE, COCAMIDOPROPYLAMINE
OXIDE, CITRIC ACID, FRAGRANCE.
PIONEER ECLIPSE TOUCHE FOAMING NON-ALCOHOL HAND
SANITIZER
benzalkonium chloride solution
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:70415-305
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 100 mL
CWGC LA Inc.
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
WATER (UNII: 059QF0KO0R)
COCO GLUCOSIDE (UNII: ICS790225B)
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)
COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
PACKAGING
# ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:70415-
305-01
1000 mL in 1 BOTTLE; Type 0: Not a Combination
Product
08/04/2017
MARKETING INFORMATION
MARKETING
CATEGORY
APPLICATION NUMBER OR MONOGRAPH
CITATION
MARKETING START
DATE
MARKETING END
DATE
OTC monograph not
final
part333E
08/04/2017
                                
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