Search by Drug Name or NDC

NDC 70888-0001-02 Antibacterial Wet Wipes 0.13 g/100g Details

Antibacterial Wet Wipes 0.13 g/100g

Antibacterial Wet Wipes is a TOPICAL SWAB in the HUMAN OTC DRUG category. It is labeled and distributed by SHAOXING BAIXUN HYGIENE PRODUCTS CO.,LTD. The primary component is BENZALKONIUM CHLORIDE.

Product Information

NDC	70888-0001
Product ID	70888-001_da8e3936-9205-730c-e053-2995a90a5a73
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Antibacterial Wet Wipes
Proprietary Name Suffix	n/a
Non-Proprietary Name	benzalkonium chloride
Product Type	HUMAN OTC DRUG
Dosage Form	SWAB
Route	TOPICAL
Active Ingredient Strength	0.13
Active Ingredient Units	g/100g
Substance Name	BENZALKONIUM CHLORIDE
Labeler Name	SHAOXING BAIXUN HYGIENE PRODUCTS CO.,LTD
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH NOT FINAL
Application Number	part333A
Listing Certified Through	2023-12-31

Package

Package Images

NDC 70888-0001-02 (70888000102)

Pricing Information	N/A
NDC Package Code	70888-001-02
Billing NDC	70888000102
Package	30 POUCH in 1 BOTTLE (70888-001-02) / .035 g in 1 POUCH
Marketing Start Date	2016-08-06
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 396303b6-3880-25b7-e054-00144ff88e88 Details

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

SPL UNCLASSIFIED SECTION

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

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TOCOPHERYL RETINOATE (UNII: 0WN694NBMM)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)

#	Item Code	Package Description	Marketing Start Date
Packaging
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 Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	08/06/2015

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

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

Revised: 3/2022

Document Id: da8e3936-9205-730c-e053-2995a90a5a73

Set id: 396303b6-3880-25b7-e054-00144ff88e88

Version: 4

Effective Time: 20220319