FDA.reportPublic FDA data

Wipex

Manufacturer
UNICO International Trading Corp. | Dan Mor
Effective date
2023-12-12
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 21:17:45

Label at a glance#

ProductWipex
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Keep out of the reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children, except with adult supervision.

Warnings

WARNINGS SECTION

For external use only. Do not use in the eyes. Keep out of eyes. In case of eye contact, rinse with water. If irritation develops, discontinue use. Consult doctor if irritation continues for more than 72 hours. If swallowed, seek medical attention or call a poison control center.

Inactice Ingredients

INACTIVE INGREDIENT SECTION

Aqua, Decyl Glucoside, Glycerin, Sodium Hydroxymethylglycinate, Citric Acid, PEG-12 Dimethicone Copolyol, Tetrasodium EDTA, Potassium Sorbate, Sodium Benzoate, Aloe Barbadensis Leaf Extract, Charmomilla Recutita (Matricaria),Flower Extract, Allantoin, Panthenol, Tocopheryl Acetate

Purpose

OTC - PURPOSE SECTION

Anti-bacterial

To Dispense

INDICATIONS & USAGE SECTION

Locate tear-notch on top of refill pouch. Tear straight across to open. Pull first wipe from center of roll through the pouch center opening. Thread wipe through dispenser nozzle. Use only upward pull dispensers.

To use

DOSAGE & ADMINISTRATION SECTION

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

Pricipal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Wipex 800 Refill PackWipex 800 Refill Pack

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74680-200-862022-06-21C16284748780-1d6a99b39-8d25-a426-e053-dadaa90af4c2Wipex
74680-200-862022-01-28C16284748780-1d6a99b39-8d25-a426-e053-dadaa90af4c2Wipex

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74680-20074680-200-86

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
SODIUM BENZOATEOJ245FE5EUIACT
SODIUM HYDROXYMETHYLGLYCINATEDIG6BWZ9XTIACT
ALOE VERA LEAFZY81Z83H0XIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
PANTHENOLWV9CM0O67ZIACT
WATER059QF0KO0RIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
CHAMOMILEFGL3685T2XIACT
ALLANTOIN344S277G0ZIACT
PEG-12 DIMETHICONE (300 CST)ZEL54N6W95IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
EDETATE SODIUMMP1J8420LUIACT
POTASSIUM SORBATE1VPU26JZZ4IACT

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
47e1e4ae-a149-07c8-e063-6394a90a6faba6807538-3ec6-22c6-e053-2995a90a4e602026-01-08WarningsExact identifier
spl set id: a6807538-3ec6-22c6-e053-2995a90a4e60

Reported adverse events (FAERS/openFDA)#

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