Covex Antibacterial Bar Fresh Protection

Manufacturer
DALAN KIMYA ENDUSTRI ANONIM SIRKETI
Effective date
2026-01-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:34:41

Label at a glance#

ProductCovex Antibacterial Bar Fresh Protection
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

for handwashing to decrease bacteria on the skin

Dosage and administration

Wet hands and forearms. Apply to hands and forearms. Scrub thoroughly for 60 seconds. Rinse and repeat

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

for handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

Do not use

OTC - DO NOT USE SECTION

  • in the eyes.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develop. If condition persists for more than 72 hours consult a doctor.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands and forearms. Apply to hands and forearms. Scrub thoroughly for 60 seconds. Rinse and repeat

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Sodium Tallowate, Sodium Palmate, Water, Sodium Palm Kernelate, Fragrance, Sodium Chloride, Glycerine, Zinc Oxide, C12-15 Alkyl Lactate, Titanium Dioxide, Tetrasodium EDTA, Etidronic Acid, Disodium Distyrylbiphenyl Disulfonate, Alpha-Isomethyl Ionone, Hexyl Cinnamal, Linalool, Limonene, Benzyl Salicylate.

Package Labeling:51209-020-90

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling:51209-020-27

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Package Labeling:51209-020-34

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2057666benzalkonium chloride 0.13 % Medicated Bar SoapPSN2
2057666benzalkonium chloride 0.0013 MG/MG Medicated Bar SoapSCD2
2057666benzalkonium chloride 0.13 % Medicated Bar SoapSY2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130739835010082GTIN-13: 0739835010082
EAN-13: 0739835010082
GTIN-12: 739835010082
UPC-A: 739835010082
GTIN storage (14 digits): 00739835010082
Label.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
07cba15c-4adc-1039-9ab9-45f5b7e84f4fProduct name120140508

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51209-020-27Covex Antibacterial Bar Fresh Protection270 g in 1 PACKAGESOAP2702
51209-020-34Covex Antibacterial Bar Fresh Protection345 g in 1 PACKAGESOAP3452
51209-020-90Covex Antibacterial Bar Fresh Protection90 g in 1 BOXSOAP902

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
51209-02051209-020-90, 51209-020-27, 51209-020-34

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 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
Covex Antibacterial Bar Fresh ProtectionBENZALKONIUM CHLORIDEDALAN KIMYA ENDUSTRI ANONIM SIRKETIbc18ed1f-1428-49c9-e053-2a95a90ac4c82026-01-22WarningsExact identifier
ndc (package): 51209-020-34
ndc (package): 51209-020-27
ndc (package): 51209-020-90
ndc (product): 51209-020
ndc11 (package): 51209002027
ndc11 (package): 51209002034
ndc11 (package): 51209002090
spl id: 48fdafc3-9a8d-5c3d-e063-6394a90a7996
spl set id: bc18ed1f-1428-49c9-e053-2a95a90ac4c8

Reported adverse events (FAERS/openFDA)#

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