FDA.reportPublic FDA data

Anti-bacterial Hand Wipes

Manufacturer
Jinhua Aidi Daily Chemical Co., Ltd.
Effective date
2026-01-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:34:56

Label at a glance#

ProductAnti-bacterial Hand Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

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

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

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

on children less than 2 months old.
on open skin wounds.

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs, These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. lf swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Propylene Glycol, Glycerin, Phenoxyethanol, Fragrance, Aloe Barbadensis Leaf Extractalky,Tocopheryl Acetate

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

20 wipes in 1 bottle NDC: 75181-012-01

20 wipes label20 wipes label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN1
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD1
1038558benzalkonium chloride 0.13 % Topical ClothSY1
1038558benzalkonium chloride 0.13 % Topical SwabSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY1
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75181-012-01Anti-bacterial Hand Wipes20 in 1 BOTTLE, PLASTICCLOTH201
75181-012-01Anti-bacterial Hand Wipes4 g in 1 PATCHCLOTH41

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75181-01275181-012-01

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
NameUNIIKind
.ALPHA.-TOCOPHEROL ACETATE, D-A7E6112E4NIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ALOE BARBADENSIS LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
PHENOXYETHANOLHIE492ZZ3TIACT
WATER059QF0KO0RIACT

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
Anti-bacterial Hand WipesANTI-BACTERIAL HAND WIPESJinhua Aidi Daily Chemical Co., Ltd.494b09a4-4982-13bf-e063-6394a90a486f2026-01-26WarningsExact identifier
ndc (package): 75181-012-01
ndc (product): 75181-012
ndc11 (package): 75181001201
spl id: 494b098d-3b9f-b54a-e063-6294a90a600c
spl set id: 494b09a4-4982-13bf-e063-6394a90a486f

Reported adverse events (FAERS/openFDA)#

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