FDA.reportPublic FDA data

Dr. C. Tuna Antibacterial Hand Wash

Manufacturer
Farmasi US LLC | TAN-ALIZE KOZMETIK VE TEMIZLIK URUNLERI SANAYI VE TICARET ANONIM SIRKETI
Effective date
2023-12-09
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:18:36

Label at a glance#

ProductDr. C. Tuna Antibacterial Hand Wash
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

wash hands and rinse

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.12%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

helps eliminate bacteria on hands

Warnings

WARNINGS SECTION

For externaluse only.

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. In case of contact, flush with water.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

except under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

wash hands and rinse

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water/Aqua, Sodium Cocoamphoacetate, Cocamidopropyl Betaine, Lauryl Glucoside, Coco-Glucoside, Glyceryl Oleate, PEG-7 Glyceryl cocoate, Styrene/Acrylates Copolymer, Glycerin, PEG/PPG-120/10 Trimethyllolpropane Trioleate, Laureth-2, Fragrance/Parfum, Sodium Benzoate, Potassium Sorbate, Citric Acid, Citral, Citronellol, geraniol, Limonene

Questions or comments?

OTC - QUESTIONS SECTION

info@farmasius.com +1 (833) 432 76 27 Monday-Friday 9 a.m-6 p.m. EST

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74690-00574690-005-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM COCOAMPHOACETATEW7Q5E87674IACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
LAURYL GLUCOSIDE76LN7P7UCUIACT
COCO GLUCOSIDEICS790225BIACT
GLYCERYL OLEATE4PC054V79PIACT
PEG-7 GLYCERYL COCOATEVNX7251543IACT
STYRENE44LJ2U959VIACT
GLYCERINPDC6A3C0OXIACT
TRIMETHYLOLPROPANE TRIOLEATES448BZW2BRIACT
LAURETH-2D4D38LT1L5IACT
SODIUM BENZOATEOJ245FE5EUIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
CITRALT7EU0O9VPPIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
GERANIOLL837108USYIACT
LIMONENE, (+)-GFD7C86Q1WIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
2914e4e9-2dd2-f40f-e063-6394a90a1b626a01591d-87c4-4908-a32e-74bd2ced700d2024-12-12WarningsExact identifier
spl set id: 6a01591d-87c4-4908-a32e-74bd2ced700d

Reported adverse events (FAERS/openFDA)#

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