Bittol Anti-Bacterial Liquid Soap

Bittol Anti-Bacterial Liquid by

Drug Labeling and Warnings

Bittol Anti-Bacterial 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 LIQUID- benzalkonium chloride liquid 
Taha Kimya Kozmetik Ve Tuketim Urunleri Sanayi Pazarlama Limited Sirketi

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Bittol Anti-Bacterial Liquid Soap

Drug Facts

Active Ingredients

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

• For handwashing to decrease bacteria on the skin.

WARNINGS

For external use only.

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:

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

Inactive Ingredients:

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 Labeling:500ml

Package Labeling:1000ml

BITTOL ANTI-BACTERIAL LIQUID 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78564-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
MYRISTAMINE OXIDE (UNII: J086PM3RRT)
COCO GLUCOSIDE (UNII: ICS790225B)
GLYCERYL OLEATE (UNII: 4PC054V79P)
GLYCERIN (UNII: PDC6A3C0OX)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78564-002-01	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/20/2020	10/31/2022
2	NDC: 78564-002-02	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/20/2020	10/31/2022
3	NDC: 78564-002-03	1000 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: 19c35ad1-c7ad-4f48-e063-6394a90a7451

34390-5

Set id: cb9a3adc-3362-43b0-8a83-eac133836bbe

Version: 3

Effective Time: 20240531

 

Taha Kimya Kozmetik Ve Tuketim U