BZK TOWELETTE- benzalkonium chloride swab

Land: USA

Språk: engelsk

Kilde: NLM (National Library of Medicine)

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Preparatomtale Preparatomtale (SPC)
13-10-2023

Aktiv ingrediens:

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

Tilgjengelig fra:

Dukal LLC

Administreringsrute:

TOPICAL

Resept typen:

OTC DRUG

Indikasjoner:

First Aid Antiseptic Antiseptic Cleansing of face, hands and body without soap and water. Air dries in seconds. In the eyes or apply over large areas of the body. If irritation, redness or other symptoms develop. Consult a doctor if the condition persists or gets worse.

Autorisasjon status:

OTC monograph not final

Preparatomtale

                                BZK TOWELETTE- BENZALKONIUM CHLORIDE SWAB
DUKAL LLC
----------
855 - BZK
_DRUG FACTS_
ACTIVE INGREDIENTS
Benzalkonium Chloride, 0.133% w/v
PURPOSE
First Aid Antiseptic
USE
Antiseptic Cleansing of face, hands and body without soap and water.
Air dries in
seconds.
DO NOT USE
In the eyes or apply over large areas of the body.
STOP USE
If irritation, redness or other symptoms develop. Consult a doctor if
the condition
persists or gets worse.
CAUTION
KEEP OUT OF REACH OF CHILDREN.
If swallowed, get medical help or contact a Poison Control Center
right away.
DIRECTIONS
Tear open packet, unfold and use as a washcloth.
INACTIVE INGREDIENTS
Sodium Bicarbonate, Water
PRINCIPAL DISPLAY PANEL - 1.4 ML POUCH LABEL
DUKAL
CORPORATION
REF 855
_NDC 65517-0004-1_
_BZK ANTISEPTIC_
_TOWELETTE_
Contains Benzalkonium Chloride
1/POUCH LATE
MANUFACTURED FOR: DUKAL CORPORATION
Ronkonkoma, NY 11779 www.dukal.com
Questions? 1-800-243-0741
Made in China D07110604 Rev7
PRINCIPAL DISPLAY PANEL - 2.1 ML POUCH LABEL
DUKAL™
CORPORATION
REF 855C
_NDC 65517-0004-2_
_NON-STERILE_
_BZK TOWELETTE_
Contains Benzalkonium Chloride
For External Use Only
1/POUCH
DUKAL CORPORATION
(631) 656-3800
Ronkonkoma, NY 11779
www.dukal.com
Made in China
BZK TOWELETTE
benzalkonium chloride swab
PRODUCT INFORMATION
Dukal LLC
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:65517-0004
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM -
UNII:7N6JUD5X6Y)
BENZ ALKONIUM
CHLORIDE
1.33 mg
in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
WATER (UNII: 059QF0KO0R)
PACKAGING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:65517-
0004-1
1.4 mL in 1 POUCH; Type 0: Not a Combination
Product
01/01/2006
2
NDC:65517-
0004-2
2.1 mL in 1 POUCH; Type 0: Not a Combination
Product
01/01/2006
MARKETING INFORMATION
MARKETING
CATEGORY
APPLICATION NUMBER OR MONOGRAPH
CITATION
MARKETING START
DATE
MARKETING END
DATE
OTC Monograph Drug
M003
01/01/
                                
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