FDA.reportPublic FDA data

Wipex

Manufacturer
Unico International Trading Corporation
Effective date
2026-01-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:31:57

Label at a glance#

ProductWipex
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

Keeo Out of the Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children. If swallowed, get medical help or contact a Poison Contrl right away.

Warning

WARNINGS SECTION

For external use only. Avoid cntact with the eyes. If in eyes, flush thoroughly with water.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Sodium benzoate, sodium chloride, citric acid, potassium sorbate, sodium hydroxymethylglycinate, aloe vera, water

Purpose

OTC - PURPOSE SECTION

Antiseptic

To disperse

INDICATIONS & USAGE SECTION

To begin: Break tab on bucket rim and pull off cover. Open bag inside to expose wipes, then thread center wipe through the lid. Replace bucket cover to maintain moisture.

Stop Use

OTC - STOP USE SECTION

Stop and ask a doctor if:

Irritation or redness developes.

Conditions persists for more than 72 hours.

To Use

DOSAGE & ADMINISTRATION SECTION

Sanitize hands or other affected area. Discard in trash after use.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Wipex 400Wipex 400

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN3
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD3
1038558benzalkonium chloride 0.13 % Topical ClothSY3
1038558benzalkonium chloride 0.13 % Topical SwabSY3
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY3
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY3
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY3

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codelinktr.ee/wipexWipex 400 201-01.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74680-201-63Wipex400 in 1 CANISTERCLOTH4003
74680-201-91Wipex2.4 mL in 1 PACKAGECLOTH2.43

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74680-20174680-201-91, 74680-201-63

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
SODIUM BENZOATEOJ245FE5EUIACT
SODIUM CHLORIDE451W47IQ8XIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
SODIUM HYDROXYMETHYLGLYCINATEDIG6BWZ9XTIACT
ALOE VERA LEAFZY81Z83H0XIACT
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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
WipexANTIBACTERIAL WIPEUnico International Trading Corporation261c7b8f-4adc-72ec-e063-6394a90a92112026-01-08WarningsExact identifier
ndc (package): 74680-201-63
ndc (package): 74680-201-91
ndc (product): 74680-201
ndc11 (package): 74680020163
ndc11 (package): 74680020191
spl id: 47e1c5f2-aa49-ae7e-e063-6294a90abf33
spl set id: 261c7b8f-4adc-72ec-e063-6394a90a9211
WipexANTIBACTERIAL WIPEUnico International Trading Corporation144453a2-8335-77be-e063-6394a90ab6762026-01-08WarningsExact identifier
ndc (package): 74680-201-91
ndc (product): 74680-201
ndc11 (package): 74680020191

Reported adverse events (FAERS/openFDA)#

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