HANDI SANI- alcohol liquid

Handi Sani by

Drug Labeling and Warnings

Handi Sani by is a Otc medication manufactured, distributed, or labeled by Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

to decrease bacteria on the skin that could cause disease
recommend for repeated use

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

Keep out of reach of children.

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 adult supervision
not recommended for infants

Other information

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

Inactive ingredients

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

SPL UNCLASSIFIED SECTION

Distributed By: Vi-Jon
8515 Page Ave
St. Louis, MO 63114

principal display panel

Handi Sani
Hand Sanitizer
Germ-X
2 FL OZ (59 mL)

INGREDIENTS AND APPEARANCE

HANDI SANI 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11344-961
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 L

Inactive Ingredients
Ingredient Name	Strength
SULISOBENZONE (UNII: 1W6L629B4K)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11344-961-16	.059 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/02/2012
2	NDC: 11344-961-18	.073 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/02/2012
3	NDC: 11344-961-21	.089 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/02/2012
4	NDC: 11344-961-34	.236 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/02/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/02/2012

Labeler - Vi-Jon (150931459)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		088520668	manufacture(11344-961)