Bittol Anti-Bacterial Hygienic Hand Cleaning Liquid

Bittol Anti-Bacterial Hygienic Hand Cleaning Liquid by

Drug Labeling and Warnings

Bittol Anti-Bacterial Hygienic Hand Cleaning Liquid by is a Otc medication manufactured, distributed, or labeled by Taha Kimya Kozmetik Ve Tuketim Urunleri Sanayi Pazarlama Limited Sirketi. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BITTOL ANTI-BACTERIAL HYGIENIC HAND CLEANING LIQUID- benzalkonium chloride liquid 
Taha Kimya Kozmetik Ve Tuketim Urunleri Sanayi Pazarlama Limited Sirketi

----------

Bittol Anti-Bacterial Hygienic Hand Cleaning Liquid

Drug Facts

Active Ingredients

Benzalkonium Chloride 0.1%

Purpose

Antibacterial

Uses

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

WARNINGS

For external use only.

Flammable, keep away from fire or flame

When using this product:

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:

Irritation and redness develops and last more than 72 hours.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.(1-800-222-1222)

Directions:

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

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

Inactive Ingredients:

Aqus/Water, Isopropyl Alcohol, Glycerin.

Package Labeling:1000ml

Package Labeling:750ml

BITTOL ANTI-BACTERIAL HYGIENIC HAND CLEANING LIQUID 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78564-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78564-003-01	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/20/2020	10/31/2022
2	NDC: 78564-003-02	750 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/20/2020	10/31/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	09/20/2020	10/31/2022

Labeler - Taha Kimya Kozmetik Ve Tuketim Urunleri Sanayi Pazarlama Limited Sirketi (565657236)

Revised: 5/2024

Document Id: 19c367d7-b7e6-20f7-e063-6394a90a332d

34390-5

Set id: 5e016ee0-6f53-42a7-ab2c-d597fbaa1db0

Version: 3

Effective Time: 20240531

 

Taha Kimya Kozmetik Ve Tuketim U