GeniusCare Antibacterial Wet Wipes

Manufacturer
RK KOZMETIK VE HIJYEN URUNLERI SANAYI DIS TICARET ANONIM SIRKETI
Effective date
2020-10-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:31:33

Label at a glance#

ProductGeniusCare Antibacterial Wet Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Indications and uses

To Dispense Wipe: Peel back front label slowly. Remove wipes. To Reseal Pouch: Firmly run thumb over the label. Do not Flush

Dosage and administration

For use by adults and children 2 years and over Use decreases bacteria on skin. Apply to hands Allow to dry without wiping

Storage and handling

DO NOT FLUSH

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

ANTIBACTERIAL WET WIPES

Perfect for quick clean-ups when soap and water are not available.

Genius Care Wet Wipes ANTIBACTERIAL SOFT GENTLE HAND WIPES

REDUCES 99.0% OF BACTERIA*

72 TRAVEL PACK THICK & SOFT CLOTHS

ALCOHOL, PARABEN & TRICLOSAN FREE

ANTIBACTERIAL WET WIPES

Travel Pack is convenient to carry for use anytime, anywhere.

*Reduces 99.9% of bacterial and fungal strains as tested in a laboratory setting ( Staphylococcus aureus)

(Pseudomonas aeruginosa)(Escherichia coli)(Enterococcus hirae)(Candida albicans)

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.1 %. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, GeniusCare

Genius Care Wet Wipes ANTIBACTERIAL SOFT GENTLE HAND WIPES

Uses

INDICATIONS & USAGE SECTION

To Dispense Wipe: Peel back front label slowly. Remove wipes.

To Reseal Pouch: Firmly run thumb over the label.

Do not Flush

Warnings

WARNINGS SECTION

For external use only.

Do not use if you are allergic to any of the ingredients

When using this product, do not get into eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

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

Ask a doctor before use

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

For use by adults and children 2 years and over

Use decreases bacteria on skin.

Apply to hands
Allow to dry without wiping

Other information

STORAGE AND HANDLING SECTION

DO NOT FLUSH

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Propylene Glycol, Cocamidopropyl Betain, PEG-7 Glyceryl Cocoate, Phenoxyethanol, Benzoic Acid, Dehydroxyacetic Acid, Fragrance, PEG-40 Hdrogenated Castor Oil, Tetrasodium EDTA, Chlorhexidin Digluconat, Citric Acid.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

​ NDC: 79320-123-01 wetwipewetwipe

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
bb6d6c68-649d-4e6d-a1f6-603d969c8f68Product name120160303

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79320-123-012022-01-28C16284748780-1d6a99b39-cb36-a426-e053-dadaa90af4c2b0c38ea3-d9ec-3198-e053-2a95a90abaf2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79320-123-01GeniusCare Antibacterial Wet Wipes59 mL in 1 BAGCLOTH592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79320-123GENIUSCARE ANTIBACTERIAL WET WIPES (BENZALKONIUM CHLORIDE) CLOTH [RK KOZMETIK VE HIJYEN URUNLERI SANAYI DIS TICARET ANONIM SIRKETI]2Legacy NDC, 1 package rows20201014_b0c38ea3-d9ec-3198-e053-2a95a90abaf2.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79320-12379320-123-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

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
b189f80c-7533-9287-e053-2a95a90a28e5b0c38ea3-d9ec-3198-e053-2a95a90abaf22020-10-13WarningsExact identifier
spl id: b189f80c-7533-9287-e053-2a95a90a28e5
spl set id: b0c38ea3-d9ec-3198-e053-2a95a90abaf2

Reported adverse events (FAERS/openFDA)#

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