VIRX HAND SANITIZER LIQUID- alcohol gel

Virx Hand Sanitizer Liquid by

Drug Labeling and Warnings

Virx Hand Sanitizer Liquid by is a Otc medication manufactured, distributed, or labeled by Filo America. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 62%

Purpose

Antimicrobial

Use

Hand sanitizer to help reduce bacteria on the skin

Warning

Flammable. Keep away from fire or flame.

For external use only.

When using this product

do not use in or near the eyes. In case of contact, rinse eyes throughtly with water.

Stop use and ask doctor if

irritation or rash appears and lasts   

Keep our of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Place enough product in your palm to throughtly cover your hands.
• Rub hands together briskly until dry.
• Children under 6 years of age should be supervied when using this product.

Other Information

• Store below 110 ​0F (45 ​0C)
• May discolor certain fabrics or surfaces.

Inactive Ingredients

Water, Isopropyl Alcohol, Aloe Barbadesis Leaf Juice, diisopropyl Sebacate, glycerin, Isopropyl Myristate, Tocopheryl Acetate, Aminomethyl Propanol, Carbomer, Fragrance (Parfum).

Package Label

INGREDIENTS AND APPEARANCE

VIRX HAND SANITIZER LIQUID 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50435-100
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
DIISOPROPYL SEBACATE (UNII: J8T3X564IH)
GLYCERIN (UNII: PDC6A3C0OX)
AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)
CARBOMER 934 (UNII: Z135WT9208)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50435-100-02	60 mL in 1 PACKAGE; Type 0: Not a Combination Product	02/08/2017
2	NDC: 50435-100-08	237 mL in 1 PACKAGE; Type 0: Not a Combination Product	02/08/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	02/08/2017

Labeler - Filo America (943873703)