BZK TOWELETTE- benzalkonium chloride swab

Land: Vereinigte Staaten

Sprache: Englisch

Quelle: NLM (National Library of Medicine)

Wirkstoff:

Benzalkonium Chloride, 0.133% w/v

Verfügbar ab:

Acme United Corporation

Verabreichungsweg:

TOPICAL

Verschreibungstyp:

OTC DRUG

Anwendungsgebiete:

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.

Berechtigungsstatus:

OTC monograph not final

Fachinformation

BZK TOWELETTE- BENZALKONIUM CHLORIDE SWAB
ACME UNITED CORPORATION
_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._
----------
FIRSAT AID ONLY BZK ANTISEPTIC TOWELETTES
_DRUG FACTS_
ACTIVE INGREDIENTS
Benzalkonium Chloride, 0.133% w/v
PURPOS E
First Aid Antiseptic
US E
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
Carton Image
BZK TOWELETTE
benzalkonium chloride swab
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:0 9 24-7112(NDC:6 5517-0 0 0 4)
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
BENZALKO NIUM CHLO RIDE (UNII: F5UM2KM3W7) (BENZALKONIUM -
UNII:7N6 JUD5X6 Y)
BENZALKONIUM
CHLORIDE
1.33 mg
in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WATER (UNII: 0 59 QF0 KO0 R)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START DATE
MARKETING END DATE
1
NDC:0 9 24-7112-0 0
1.4 mL in 1 POUCH; Type 0 : No t a Co mbinatio n Pro duct
0 4/16 /20 19
2
NDC:0 9 24-7112-0 1
10 in 1 CARTON
0 4/16 /20 19
2
1.4 mL in 1 POUCH; Type 0 : No t a Co mbinatio n Pro duct
3
NDC:0 9 24-7112-0 2
10 in 1 CARTON
0 4/16 /20 19
3
1.4 mL in 1 POUCH; Type 0 : No t a Co mbinatio n Pro duct
4
NDC:0 9 24-7112-0 3
25 in 1 CARTON
0 4/16 /20 19
4
1.4 mL in 1 POUCH; Type 0 : No t a Co mbinatio n Pro duct
5
NDC:0 9 24-7112-0 4
50 in 1 CARTON
0 4/16 /20 19
5
1.4 mL in 1 POUCH; Type 0 : No t a Co mbinatio n Pro duc