VIRAPRO ZERO HAND CLEANSER- benzalkonium chloride gel

VIRAPRO ZERO HAND CLEANSER by

Drug Labeling and Warnings

VIRAPRO ZERO HAND CLEANSER by is a Otc medication manufactured, distributed, or labeled by ALL ONE KOZMETIK SANAYI DIS TICARET ANONIM SIRKETI, HARDAL GLOBAL CONSULTING LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Benzalkonium Chloride 0.01% w/w

Purpose

Antiseptic Hand Sanitizer

Use

Used for general purpose hand and skin sanitization. Suitable for children. Can be used at home, school, kindergarten, or hospital. Keeps hands soft with its moisturizer content.

Warnings

For external use only.

WHEN USING

When using this product, avoid contact with the eyes. In case of contact with eyes, rinse eyes thoroughly with water.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children under 3 years of age. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Squeeze a drop onto the palm of your hands. Rub your hands well and let them dry.

Inactive ingredients

Aqua, Glycerin, Triethanolamine, Carbomer, Mint extract

Other information

Store between 15-30 °C (59-86 °F). Avoid freezing or excessive heat above 40 °C (104 °F).

Shelf life of the product is 2 years. Once opened, use within 3 months.

DISPOSAL AND WASTE HANDLING

Dispose of contents/bottle in accordance with local regulations.

Package Label - Principal Display Panel

virapro

ZERO

0% ALCOHOL

Dermal Disinfectant

HAND CLEANSER GEL

For external use only

Mint

Rinse free protection on-the-go

U.S. Contact: ViraPro North America
550 Albion Ave. Schaumburg Chicago, IL 60193
Phone: +1 (312) 340-0288
www.viapro.com

Manufacturer: All One Kozmetik

Sutluce, Imrahor Cd. No:36, 34445 Beyoglu/Istanbul

Phone: (0212) 501 19 00

MADE IN EUROPE
https://www.allone.com.tr/

INGREDIENTS AND APPEARANCE

VIRAPRO ZERO HAND CLEANSER 
benzalkonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75348-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.01 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER 980 (UNII: 4Q93RCW27E)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75348-005-01	100 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/30/2020

Labeler - ALL ONE KOZMETIK SANAYI DIS TICARET ANONIM SIRKETI (519983719)

Registrant - HARDAL GLOBAL CONSULTING LLC. (123584960)

Establishment
Name	Address	ID/FEI	Business Operations
ALL ONE KOZMETIK SANAYI DIS TICARET ANONIM SIRKETI		519983719	manufacture(75348-005)