FDA.reportPublic FDA data

Antibacterial Hand Wipe

Manufacturer
Fujian Yifa Healthcare Products Co., Ltd.
Effective date
2025-06-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:03:43

Label at a glance#

ProductAntibacterial Hand Wipe
Active ingredientBENZALKONIUM CHLORIDE
Label structure21 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.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

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

Aloe Barbadensis Leaf Extract,Alpha-Tocopherol,Fragrance,Glycerin,Phenoexyethanol,Propylene Glycol,Water.

Questions

OTC - QUESTIONS SECTION

call 718-975-2586

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

75543-301-0111

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

75543-301-0222

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

75543-301-0333

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

75543-301-04

44

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

75543-301-0555

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

75543-301-0666

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

75543-301-0777

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

75543-301-0888

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75543-301-01Antibacterial Hand Wipe40 in 1 PATCHPATCH401
75543-301-02Antibacterial Hand Wipe40 in 1 PATCHPATCH401
75543-301-03Antibacterial Hand Wipe40 in 1 PATCHPATCH401
75543-301-04Antibacterial Hand Wipe40 in 1 PATCHPATCH401
75543-301-05Antibacterial Hand Wipe40 in 1 PATCHPATCH401
75543-301-06Antibacterial Hand Wipe40 in 1 PATCHPATCH401
75543-301-07Antibacterial Hand Wipe40 in 1 PATCHPATCH401
75543-301-08Antibacterial Hand Wipe40 in 1 PATCHPATCH401

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75543-30175543-301-01, 75543-301-02, 75543-301-03, 75543-301-04, 75543-301-05, 75543-301-06, 75543-301-07, 75543-301-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPYLENE GLYCOL6DC9Q167V3IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ALOE BARBADENSIS LEAFZY81Z83H0XIACT
PHENOXYETHANOLHIE492ZZ3TIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ALPHA-TOCOPHEROLH4N855PNZ1IACT
FRAGRANCE 135765EM498GW35IACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Antibacterial Hand WipeANTIBACTERIAL HAND WIPEFujian Yifa Healthcare Products Co., Ltd.38381a41-db33-45c6-e063-6394a90a23172025-06-23WarningsExact identifier
ndc (package): 75543-301-03
ndc (package): 75543-301-06
ndc (package): 75543-301-01
ndc (package): 75543-301-04
ndc (package): 75543-301-05
ndc (package): 75543-301-08
ndc (package): 75543-301-02
ndc (package): 75543-301-07
ndc (product): 75543-301
ndc11 (package): 75543030107
ndc11 (package): 75543030102
ndc11 (package): 75543030104
ndc11 (package): 75543030106
ndc11 (package): 75543030108
ndc11 (package): 75543030105
ndc11 (package): 75543030103
ndc11 (package): 75543030101
spl id: 38381a41-db34-45c6-e063-6394a90a2317
spl set id: 38381a41-db33-45c6-e063-6394a90a2317

Reported adverse events (FAERS/openFDA)#

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