ANTIBACTERIAL WET WIPES- benzalkonium chloride swab

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

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

Available from:

Zhejiang Qimei Commodity Co.,Ltd.

INN (International Name):

BENZALKONIUM CHLORIDE

Composition:

BENZALKONIUM CHLORIDE 0.13 g in 100 g

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

Antibacterial for hand washing to decrease bacteria on skin

Authorization status:

OTC monograph not final

Summary of Product characteristics

ANTIBACTERIAL WET WIPES- BENZALKONIUM CHLORIDE SWAB
ZHEJIANG QIMEI COMMODITY CO.,LTD.
_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._
----------
69821-001 ANTIBACTERIAL WET WIPES
ACTIVE INGREDIENT
benzalkonium chloride 0.13%
PURPOSE
Antibacterial
USES
for hand washing to decrease bacteria on skin
WARNINGS
For External use only.
Do not use if you are allergic to any of the ingredients.
When using this product Do not get into eyes,if contact occurs ,rinse
throughly with
water.
Discontinue use if irritation or redness develops if condition
persists for more than 72
hours consults a physician.
KEEP OUT OF REACH OF CHILDREN
keep out of reach of children unless under adult supervision .if
seallowed ,get medical
help or contact a Poison Control Center immediately.
DIRECTIONS
Thoroughly wipe hands or face with wipe,Discard in trash receptacle;do
not flush.Be
sure to reseal label complete to retain moisture
WATER PROPYLENE GLYCOL OCTHILINONE .ALPHA.-TOCOPHEROL
ANTIBACTERIAL WET WIPES
benzalkonium chloride swab
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:69821-001
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 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TOCOPHERYL RETINOATE (UNII: 0WN694NBMM)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
PACKAGING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:69821-
001-01
10 in 1 PACKAGE
06/01/2017
1
0.0042 g in 1 POUCH; Type 0: Not a Combination
Product
2
NDC:69821-
001-02
15 in 1 PACKAGE
06/01/2017
2
0.0042 g in 1 POUCH; Type 0: Not a Combination
2
Product
3
NDC:6