FDA.reportPublic FDA data

Wonvia Antibacterial Wipes

Manufacturer
Kaplan Distribution LLC | HARDAL GLOBAL CONSULTING LLC | RKS GROUP YAPI KIMYASALLARI SANAYI VE TICARET LIMITED SIRKETI
Effective date
2020-08-12
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:24:57

Label at a glance#

ProductWonvia Antibacterial Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure13 sections

Storage and handling

Keep away from sunlight or direct heat and store at room temperature.

Label contents#

Full prescribing information#

DESCRIPTION SECTION

Wonvia antibacterial wipes

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Active material name and amount (%): (Chemical Name; CAS No.) Benzalkonium Chloride %0,23 (CAS NO: 68424-85-1)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive material name: Aqua, Olus Oil, Lauryl Glucoside, Glycerin, Propylene Glycol, Polyglyceryl-2 Dipolyhydroxystearate, Phenoxyethanol, Parfum, Polysorbate 20, Glyceryl Oleate, Dicaprylyl Carbonate, Dehdroacetic Acid, Benzoic Acid, Tetrasodium EDTA, Benzyl Alcohol, Benzyl Salicylate, Citronellol, Coumarin, Linalool.

Purpose

OTC - PURPOSE SECTION

Antibacterial Wet Wipes.

DOSAGE & ADMINISTRATION SECTION

It is illegal to use this product for uses or in a manner other than prescribed on this label

Use

INDICATIONS & USAGE SECTION

Antibacterial Wet Wipes. Cleans and softens the skin and provides a pleasant odor.

Warnings

WARNINGS SECTION

Non-edible.

Do not use

OTC - DO NOT USE SECTION

Do not use on eyes.

STORAGE AND HANDLING SECTION

Keep away from sunlight or direct heat and store at room temperature.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

DISPOSAL AND WASTE HANDLING

Dispose of contents/container in accordance with local regulations.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

WONVIA antibacterial

antibacterial wipes

kills 99,9% of bacteria

120 wipes

effective hygiene wipes

Use biocides safely and sustainably.

Production date, expiry date and batch number are on the pack.

Kaplan Distribution LLC

828 N. OLDEN AVE. TRENTON, NJ 08638 USA

Made in Turkey

7272120120

Produced under hygienic environment and conditions according to ISO 22716:2007 (GMP) and ISO 9001:2015 Quality Management System.

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2375303benzalkonium chloride 0.23 % Medicated PadPSN3
2375303benzalkonium chloride 2.3 MG/ML Medicated PadSCD3
2375303benzalkonium chloride 0.23 % Medicated PadSY3

DailyMed Product Concepts#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78876-707-122022-01-28C16284748780-1d6a99b39-fa06-a426-e053-dadaa90af4c2a8399fc9-2bd3-8e84-e053-2995a90a3023
78876-707-722022-01-28C16284748780-1d6a99b39-fa06-a426-e053-dadaa90af4c2a8399fc9-2bd3-8e84-e053-2995a90a3023

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78876-707-12Wonvia Antibacterial Wipes460 g in 1 PACKAGECLOTH4603
78876-707-72Wonvia Antibacterial Wipes335 g in 1 PACKAGECLOTH3353

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78876-707WONVIA ANTIBACTERIAL WIPES (BENZALKONIUM CHLORIDE) CLOTH [KAPLAN DISTRIBUTION LLC]3Legacy NDC, 2 package rows20200818_a8399fc9-2bd3-8e84-e053-2995a90a3023.zip

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78876-70778876-707-72, 78876-707-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
POLYSORBATE 207T1F30V5YHIACT
BENZOIC ACID8SKN0B0MIMIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
BENZYL ALCOHOLLKG8494WBHIACT
COUMARINA4VZ22K1WTIACT
LINALOOL, (+)-F4VNO44C09IACT
DICAPRYLYL CARBONATE609A3V1SUAIACT
EDETATE SODIUMMP1J8420LUIACT
BENZYL SALICYLATEWAO5MNK9TUIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
LAURYL GLUCOSIDE76LN7P7UCUIACT
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE9229XJ4V12IACT
PHENOXYETHANOLHIE492ZZ3TIACT
GLYCERYL OLEATE4PC054V79PIACT
DEHYDROACETIC ACID2KAG279R6RIACT

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
acb52ee1-b939-86a5-e053-2a95a90aeafba8399fc9-2bd3-8e84-e053-2995a90a30232020-08-12WarningsExact identifier
spl id: acb52ee1-b939-86a5-e053-2a95a90aeafb
spl set id: a8399fc9-2bd3-8e84-e053-2995a90a3023

Reported adverse events (FAERS/openFDA)#

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