DR. C. TUNA ANTIBACTERIAL LIQUID HAND SANITIZER LEMON- alcohol liquid

Dr. C. Tuna Antibacterial Liquid Hand Sanitizer Lemon by

Drug Labeling and Warnings

Dr. C. Tuna Antibacterial Liquid Hand Sanitizer Lemon by is a Otc medication manufactured, distributed, or labeled by Farmasi US LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Ethyl Alcohol 80% v/v

Purpose

Antiseptic

Use[s]

Liquid Hand Sanitizer helps to reduce bacteria on the skin.

Warnings

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

Do not use

• on children under 2 months of age
• on irritated and 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 15-30ºC ( 59-86ºF )
• Avoid freezing and excessive heat above 40ºC (104ºF)

Inactive ingredients:

Water/Aqua, Fragrance/Parfum, Camellia Sinensis Leaf Extract, Aloe Barbadensis Leaf Juice, Citral, Limonene, Linalool.

Package Labeling:

INGREDIENTS AND APPEARANCE

DR. C. TUNA ANTIBACTERIAL LIQUID HAND SANITIZER LEMON 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74690-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.8 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CITRAL (UNII: T7EU0O9VPP)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
LINALOOL, (+/-)- (UNII: D81QY6I88E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74690-007-01	1 in 1 BOX	12/01/2020
1		115 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	12/01/2020

Labeler - Farmasi US LLC (113303351)