HAND SANITIZER- alcohol lotion

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Vi-Jon, Inc, Vi-Jon. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl alcohol 62%

Purpose

Antiseptic

Use

for handwashing to decrease bacteria on the skin.

Warnings

for external use only-hands

Flammable

Keep away from heat and flame.

When using this product

• keep out of eyes.  In case of contact with eyes, flush thoroughly with water
• avoid contact with broken skin
• do not inhale or ingest

Stop use and ask a doctor if

skin irritation develops

Stop use and ask a doctor if

stop use and ask a doctor if swallowed get medical help or contact a Poison Control Center right away.

Directions

• wet hands thoroughly with product and allow to dry without wiping
• for children under 6, use only under adult supervision
• not recommended for infants

Other information

• do not store above 105⁰ F
• may discolor some fabrics
• harmful to wood finishes ad plastics

Inactive ingredients

benzophenone-4, blue 1, carbomer, fragrance, glycerin, isopropyl alcohol, isopropyl myristate, red 33, tocopheryl acetate, water

Adverse Reaction

Distributed by 

Vi-Jon, Inc

8515 Page Ave

St. Louis, MO 63114

PRINCIPAL DISPLAY PANEL

NDC: 11344-616-18

Blastin' Blueberry

germ blaster

HAND SANITIZER

germ-X

KILLS 99.99% OF GERMS

2.5 FL OZ (73 mL)

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11344-616
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11344-616-18	73 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/19/2005

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/19/2005

Labeler - Vi-Jon, Inc (150931459)

Registrant - Vi-Jon (150931459)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		150931459	manufacture(11344-616)