FDA.reportPublic FDA data

Bittol Anti-Bacterial Liquid

Manufacturer
Taha Kimya Kozmetik Ve Tuketim Urunleri Sanayi Pazarlama Limited Sirketi
Effective date
2023-12-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:18:23

Label at a glance#

ProductBittol Anti-Bacterial Liquid
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

For handwashing to decrease bacteria on the skin.

Dosage and administration

The pump to get some up Bittol Antibacterial Liquid Soap on your hand,lather it and wash your hands with very will.

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 in or near the eyes. In case of eye contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if:

OTC - STOP USE SECTION

Irritation and redness develops and last more than 72 hours.

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.(1-800-222-1222)

Directions:

DOSAGE & ADMINISTRATION SECTION

The pump to get some up Bittol Antibacterial Liquid Soap on your hand,lather it and wash your hands with very will.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Aqua/Water, Lauramine Oxide, PEG-150 Distearate, Cetrimonium Chloride, Myristamine Oxide, Coco-Glucoside, Glyceryl Oleate, Glycerin, Parfum/Fragrance, Disodium EDTA, Sodium Chloride, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone, FD&C Yellow 5.

Package Labeling:250ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Package Labeling:500ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

Package Labeling:1000ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle3Bottle3

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78564-00278564-002-01, 78564-002-02, 78564-002-03

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
WATER059QF0KO0RIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
PEG-150 DISTEARATE6F36Q0I0ACIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
MYRISTAMINE OXIDEJ086PM3RRTIACT
COCO GLUCOSIDEICS790225BIACT
GLYCERYL OLEATE4PC054V79PIACT
GLYCERINPDC6A3C0OXIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
SODIUM CHLORIDE451W47IQ8XIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
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
19c35ad1-c7ad-4f48-e063-6394a90a7451cb9a3adc-3362-43b0-8a83-eac133836bbe2024-05-31WarningsExact identifier
spl set id: cb9a3adc-3362-43b0-8a83-eac133836bbe

Reported adverse events (FAERS/openFDA)#

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