Bittol Anti-Bacterial Wet Wipes

Manufacturer
Taha Kimya Kozmetik Ve Tuketim Urunleri Sanayi Pazarlama Limited Sirketi
Effective date
2023-12-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:17:41

Label at a glance#

ProductBittol Anti-Bacterial Wet Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Indications and uses

decreases bacteria on skin.

Dosage and administration

Removelid and open the seal. Pull up the corner of the center sheet, twist and thread through the dispenser split in the lid. Pull sheet out at an angle. When finished close lid flap to retain moisture.

Label contents#

Full prescribing information#

Active Ingredient (by volume)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride % 0.13

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

  • decreases bacteria on skin.

WARNINGS

WARNINGS SECTION

For external use only

Do not use:

OTC - DO NOT USE SECTION

Over large areas of the body if you are allergic to any of the ingredients.

When using this product

OTC - WHEN USING SECTION

do not get into eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor 

OTC - STOP USE SECTION

if irritation or rash develops and continues for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

For children under 2 years ask a doctor before use. For children use under adult supervision.

Directions

DOSAGE & ADMINISTRATION SECTION

Removelid and open the seal. Pull up the corner of the center sheet, twist and thread through the dispenser split in the lid. Pull sheet out at an angle. When finished close lid flap to retain moisture.

Other Information:

SPL UNCLASSIFIED SECTION

Do not expose to direct sunlight, preferably place them in a cool place. Do not use on furniture. Do not flush down toilets, dispose in trash can.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Aqua, Glycerin, Phenoxyethanol, Parfum, Polysorbate 20, Sodium PCA, Tetrasodium EDTA, Ethylhexylglycerin, Citric Acid.

Package Labeling:10 Count

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Package Labeling:40 Count

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

Package Labeling:72 Count

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle3Bottle3

Package Labeling:100 Count

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle4Bottle4

Package Labeling:120 Count

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle5Bottle5

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78564-00078564-000-01, 78564-000-02, 78564-000-03, 78564-000-04, 78564-000-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
19c34213-51e2-79a8-e063-6394a90a92bd24d91fdf-3b2e-4c9c-b0a8-c6f593476e0e2024-05-31WarningsExact identifier
spl set id: 24d91fdf-3b2e-4c9c-b0a8-c6f593476e0e

Reported adverse events (FAERS/openFDA)#

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