BZK PADS- benzalkonium chloride swab

Land: USA

Språk: engelska

Källa: NLM (National Library of Medicine)

Aktiva substanser:

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

Tillgänglig från:

Dynarex Corporation

Administreringssätt:

TOPICAL

Receptbelagda typ:

OTC DRUG

Terapeutiska indikationer:

First Aid Antiseptic • For perineal and maternity care throughout postpartum and whenever refreshing is needed.

Bemyndigande status:

OTC monograph not final

Produktens egenskaper

BZK PADS- BENZALKONIUM CHLORIDE SWAB
DYNAREX 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._
----------
1302 CLEANSING TOWELETTES NDC 67777-244-01
_ACTIVE INGREDIENT_
Benzalkonium Chloride 0.13% v/v
_PURPOSE_
First Aid Antiseptic
_USES_
• For perineal and maternity care throughout postpartum and whenever
refreshing is
needed.
_WARNINGS_
FOR EXTERNAL USE ONLY
_DO NOT USE_
• In the eye
_STOP USE AND ASK A DOCTOR IF_
• Irritation and redness develop
• If condition persists for gets worse
_KEEP OUT OF REACH OF CHILDREN_
If swallowed, get medical help or contact a Poison Control Center
(1-800-222-1222)
right away.
_DIRECTIONS_
• Unfold towel
• Cleanse the desired area
• Dispose of towlette after single use.
_OTHER INFORMATION_
• Store at room temperature 15º-30ºC (59º-86ºF)
• Avoid excessive heat.
• Tamper evident. Do not use if packet is torn or cut.
_INACTIVE INGREDIENTS_
Chlorothymol, Isopropyl Acohol, Water, may contain
Methylchloroisothiazolinone/Methylisothiazolinone
_LABEL_
1302 Label
_LABEL_
1302 Obstetrical Towelette
BZK PADS
benzalkonium chloride swab
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:67777-244
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM -
UNII:7N6JUD5X6Y)
BENZ ALKONIUM
CHLORIDE
1.3 mg
in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
METHYLCHLOROISOTHIAZOLINONE/METHYLISOTHIAZOLINONE MIXTURE (UNII:
15O9QS218W)
CHLOROTHYMOL (UNII: LJ25TI0CVT)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
WATER (UNII: 059QF0KO0R)
Dynarex Corporation
PACKAGING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:67777-244-
01
10 in 1 CASE
04/05/2011
1
NDC:67777-244-
02
100 in 1 BOX
1
0.55 mL in 1 PACKET; Type 0: Not a Combination
Product
MARKETING INFORMATION
MA