BIOPURE Antibacterial Hand Wipes-Unscented

Manufacturer: Fujian Yifa Healthcare Products Co., Ltd.
Effective date: 2026-03-25
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:51:42

Label at a glance#

ProductAntibacterial Hand Wipe

Active ingredientBENZALKONIUM CHLORIDE

Label structure14 sections

Dosage and administration

1.Apply to hands,allow to air dry without wiping; 2.Children under 6 years of age should be supervised when using this product.

Storage and handling

1.Store in a cool,dry place;2.Avoid freezing and excessive heat.

Contacts and useful links#

PhoneLabel contact718-975-2586

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.12%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria;
For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

In children less than 2 months old;
On open skin wounds.

When Using

OTC - WHEN USING SECTION

keep out of eyes,ears,and mouth.In case of contact with eyes,rinse eyes thoroughly with water.

Stop Use

OTC - STOP USE SECTION

If irritation or rash occurs.These may be signs of a serious condition.

Ask Doctor

OTC - ASK DOCTOR SECTION

If irritation or rash occurs.These may be signs of a serious condition.

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

1.Apply to hands,allow to air dry without wiping;
2.Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

1.Store in a cool,dry place;2.Avoid freezing and excessive heat.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Propylene Glycol, Ethylhexylglycerin, Phenoexyethanol, Didecyldimonium Chloride

Questions

OTC - QUESTIONS SECTION

call 718-975-2586

PRINCIPAL DISPLAY PANEL-77543-312-00

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Antiseptic Wipe

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0810146468127	GTIN-13: 0810146468127 EAN-13: 0810146468127 GTIN-12: 810146468127 UPC-A: 810146468127 GTIN storage (14 digits): 00810146468127	BZK Hand Wipe Pack.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75543-312-00	Antibacterial Hand Wipe	1 in 1 PACKAGE	CLOTH	1		1
75543-312-00	Antibacterial Hand Wipe	72 in 1 BOX	CLOTH	72		1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

Antibacterial Hand Wipe
DIDECYLDIMONIUM CHLORIDE
PROPYLENE GLYCOL
PHENOXYETHANOL
WATER
GLYCERIN
BENZALKONIUM CHLORIDE
BENZALKONIUM
ETHYLHEXYLGLYCERIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75543-312	75543-312-00

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
DIDECYLDIMONIUM CHLORIDE	JXN40O9Y9B	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
ETHYLHEXYLGLYCERIN	147D247K3P	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Antibacterial Hand Wipe	ANTIBACTERIAL HAND WIPE	Fujian Yifa Healthcare Products Co., Ltd.	4dde3373-1c75-a815-e063-6294a90aa557	2026-03-25	Warnings	Exact identifier ndc (package): 75543-312-00 ndc (product): 75543-312 ndc11 (package): 75543031200 spl id: 4dde300d-240c-8e06-e063-6294a90a417b spl set id: 4dde3373-1c75-a815-e063-6294a90aa557

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.