ANTIBACTERIAL WET WIPES- benzalkonium chloride swab

Antibacterial Wet Wipes by

Drug Labeling and Warnings

Antibacterial Wet Wipes by is a Otc medication manufactured, distributed, or labeled by SHAOXING BAIXUN HYGIENE PRODUCTS CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INACTIVE INGREDIENT

WATER PROPYLENE GLYCOL OCTHILINONE .ALPHA.-TOCOPHEROL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL WET WIPES 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70888-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM 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: 70888-001-01	15 in 1 PACKAGE	08/06/2016
1		0.06 g in 1 POUCH; Type 0: Not a Combination Product
2	NDC: 70888-001-02	30 in 1 BOTTLE	08/06/2016
2		0.035 g in 1 POUCH; Type 0: Not a Combination Product
3	NDC: 70888-001-03	10 in 1 PACKAGE	08/06/2016
3		0.042 g in 1 POUCH; Type 0: Not a Combination Product
4	NDC: 70888-001-04	30 in 1 PACKAGE	08/06/2016
4		0.126 g in 1 POUCH; Type 0: Not a Combination Product
5	NDC: 70888-001-05	50 in 1 PACKAGE	08/06/2016
5		0.21 g in 1 POUCH; Type 0: Not a Combination Product
6	NDC: 70888-001-06	80 in 1 PACKAGE	08/06/2016
6		0.336 g in 1 POUCH; Type 0: Not a Combination Product
7	NDC: 70888-001-07	100 in 1 PACKAGE	08/06/2016
7		0.42 g in 1 POUCH; Type 0: Not a Combination Product
8	NDC: 70888-001-08	50 in 1 BOTTLE	08/06/2016
8		0.21 g in 1 POUCH; Type 0: Not a Combination Product
9	NDC: 70888-001-09	80 in 1 BOTTLE	08/06/2016
9		0.336 g in 1 POUCH; Type 0: Not a Combination Product
10	NDC: 70888-001-10	100 in 1 BOTTLE	08/06/2016
10		0.42 g in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/06/2015

Labeler - SHAOXING BAIXUN HYGIENE PRODUCTS CO.,LTD (544419193)

Establishment
Name	Address	ID/FEI	Business Operations
SHAOXING BAIXUN HYGIENE PRODUCTS CO.,LTD		544419193	manufacture(70888-001)