Bittol Anti-Bacterial Hygienic Hand Cleaning 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 21:18:17

Label at a glance#

ProductBittol Anti-Bacterial Hygienic Hand Cleaning Liquid
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

To decrease bacteria on the skin. When water, soap & towel are not available. Recommended for repeated use

Dosage and administration

Remove all your jewelry before use. Be careful to there is no visible dirtiness on the hands and make should that hands and skin not wet. Take 3-5 ml of Bittol Antibacterial Hygienic Hand Cleaning Liquid. Rub hands until it is dry properly.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

  • To decrease bacteria on the skin.
  • When water, soap & towel are not available.
  • Recommended for repeated use

WARNINGS

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame

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

Remove all your jewelry before use. Be careful to there is no visible dirtiness on the hands and make should that hands and skin not wet. Take 3-5 ml of Bittol Antibacterial Hygienic Hand Cleaning Liquid. Rub hands until it is dry properly.

Other Information

SPL UNCLASSIFIED SECTION

  • Store below 110°F (43°C)
  • May discolor certain fabrics or surfaces.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Aqus/Water, Isopropyl Alcohol, Glycerin.

Package Labeling:1000ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BoxBox

Package Labeling:750ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Box2Box2

Products#

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DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78564-00378564-003-01, 78564-003-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
19c367d7-b7e6-20f7-e063-6394a90a332d5e016ee0-6f53-42a7-ab2c-d597fbaa1db02024-05-31WarningsExact identifier
spl set id: 5e016ee0-6f53-42a7-ab2c-d597fbaa1db0

Reported adverse events (FAERS/openFDA)#

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