Bittol Anti-Bacterial Hand Gel

Bittol Anti-Bacterial Hand Gel by

Drug Labeling and Warnings

Bittol Anti-Bacterial Hand Gel 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 HAND GEL- alcohol gel 
Taha Kimya Kozmetik Ve Tuketim Urunleri Sanayi Pazarlama Limited Sirketi

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Bittol Anti-Bacterial Hand Gel

Drug Facts

Active Ingredients

Ethyl Alcohol 70%

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.

Directions:

Provides practical cleaning without using water and soap when necessary. It used for hand cleaning. Remove all your jewerly before use. Be careful to there is no visible dirtiness on the hands and that the hands skin are not wet. It used as often as desired. Take 3-5 ml of Bittol Antibacterial Hand Gel. Rub your hands with Bittol Antibacterial Hand gel Until it is dry properly. Children under 6 years of age should be supervised when using this product.

Other Information:

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

Inactive Ingredients:

Aqua/Water, Carbomer, Glycerin, Triethanolamine, Parfum/Fragrance.

Package Labeling:100ml

Package Labeling:250ml

Package Labeling:500ml

BITTOL ANTI-BACTERIAL HAND GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78564-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78564-001-01	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/14/2020	10/31/2022
2	NDC: 78564-001-02	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/14/2020	10/31/2022
3	NDC: 78564-001-03	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/14/2020	10/31/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	08/14/2020	10/31/2022

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

Revised: 5/2024

Document Id: 19c34213-51ea-79a8-e063-6394a90a92bd

34390-5

Set id: aa4fb388-95df-4d66-9e56-0ebd9009c87d

Version: 5

Effective Time: 20240531

 

Taha Kimya Kozmetik Ve Tuketim U