Bittol Alcohol Wipes by Taha Kimya Kozmetik Ve Tuketim Urunleri Sanayi Pazarlama Limited Sirketi Bittol Alcohol Wipes

Bittol Alcohol Wipes by

Drug Labeling and Warnings

Bittol Alcohol Wipes 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 ALCOHOL WIPES- alcohol cloth 
Taha Kimya Kozmetik Ve Tuketim Urunleri Sanayi Pazarlama Limited Sirketi

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Bittol Alcohol Wipes

Drug Facts

Active Ingredients

Ethyl Alcohol 75%

Purpose

Antimicrobial

Uses

• For hand and skin sanitizing.
• 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.
• Use wipes only on unbroken intact skin.
• If you have sensitive skin or certain allergies, check the list of ingredients on the label before using wipes.
• Do not ingest. 

Stop use and ask a doctor:

If skin irritation or redness develops.

Directions:

• Children under 6 years of age use only under adult supervision. Keep out of reach of children.
• If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)
• Not recommended for infants.

Keep out of reach of children.

Children under 6 years of age use only under adult supervision.

Other Information:

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

Inactive Ingredients:

Aqua/ Water, Glycerin, Propylene Glycol, Parfum/ Fragrance, Sodium PCA, Disodium EDTA.

Package Labeling:40 Count

Package Labeling:80 Count

Package Labeling:100 Count

Package Labeling:120 Count

Package Labeling:150 Count

BITTOL ALCOHOL WIPES 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78564-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.75 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78564-004-01	40 in 1 CANISTER	11/01/2020	11/02/2020
1		3.1 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2	NDC: 78564-004-02	80 in 1 CANISTER	11/01/2020	11/02/2020
2		3.1 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
3	NDC: 78564-004-03	100 in 1 CANISTER	11/01/2020	11/02/2020
3		3.1 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
4	NDC: 78564-004-04	120 in 1 CANISTER	11/01/2020	11/02/2020
4		3.1 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
5	NDC: 78564-004-05	150 in 1 CANISTER	11/01/2020	11/02/2020
5		3.1 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	11/01/2020	11/02/2020

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

Revised: 5/2024

Document Id: 19c37dc3-80b3-5b99-e063-6294a90adf3c

34390-5

Set id: 07a47fd5-ac48-4ff9-8a16-0a4cb15e3c3d

Version: 3

Effective Time: 20240531

 

Taha Kimya Kozmetik Ve Tuketim U