Dr. C. Tuna Antibacterial Waterless Hand Sanitizer

Dr. C. Tuna Antibacterial Waterless Hand Sanitizer by

Drug Labeling and Warnings

Dr. C. Tuna Antibacterial Waterless Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Farmasi US LLC, TAN-ALIZE KOZMETIK VE TEMIZLIK URUNLERI SANAYI VE TICARET ANONIM SIRKETI. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DR. C. TUNA ANTIBACTERIAL WATERLESS HAND SANITIZER- alcohol gel 
Farmasi US LLC

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Dr. C. Tuna Antibacterial Waterless Hand Sanitizer

Drug Facts

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Use[s]

Health care personnel hand rub to help reduce bacteria that potentially can cause disease.

Warnings

For external use only. Flammable. Keep away from heat or flame.

Do not use

• in children less than 2 months of age
• on open skin wounds

When using this product

keep out of eyes, ears, and mouth. In case of contact with eyes. rinse eyes thoroughly with water. 

Stop use and ask a doctor

if irritation or rash occurs. These may be signs of a serious condition. 

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Place enough product on hands to cover all surfaces. Rub hands together until dry. 
• Supervise children under 6 years of age when using this product to avoid swallowing. 

Other information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

Propylene Glycol, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Isopropyl Alcohol, Carbomer, Triethanolamine, Tocopheryl Acetate, Purified Water USP

Package Labeling

DR. C. TUNA ANTIBACTERIAL WATERLESS HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74690-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
TROLAMINE (UNII: 9O3K93S3TK)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74690-004-01	75 mL in 1 TUBE; Type 0: Not a Combination Product	06/15/2020	09/30/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	06/15/2020	09/30/2023

Labeler - Farmasi US LLC (113303351)

Establishment
Name	Address	ID/FEI	Business Operations
TAN-ALIZE KOZMETIK VE TEMIZLIK URUNLERI SANAYI VE TICARET ANONIM SIRKETI		365979587	manufacture(74690-004)

Revised: 12/2024

Document Id: 2914d228-e0f4-fa38-e063-6294a90a9778

34390-5

Set id: 21963da9-9885-488d-9f7c-cc14a48d2a6b

Version: 4

Effective Time: 20241212